# SNPedia annotations # http://www.snpedia.com/files/snpedia # Date: Tue Sep 9 01:44:44 2008 [general] glyph=triangle point=1 orient=N description=1 key=SNPedia annotation label=1 fgcolor=black section=region [illumina] key=snp (illumina) bgcolor=#FF0000 [both] key=snp (affy;illumina) bgcolor=#C000C0 [affy] key=snp (affy) bgcolor=#0000FF [snp] key=snp () bgcolor=grey reference = Chr11 illumina rs1001179 34416807..34416807 "A study of non-Hispanic Caucasians with various types of brain tumors concluded that there was an de..." http://www.snpedia.com/index.php?title=Rs1001179 reference = Chr4 both rs10012946 6344251..6344251 "rs10012946 is in linkage disequilibrium with a polymorphism that increases susceptibility to Type II..." http://www.snpedia.com/index.php?title=Rs10012946 reference = ChrNone illumina rs10025771 69087820..69087820 "Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable...." http://www.snpedia.com/index.php?title=Rs10025771 reference = Chr4 snp rs10029345 35958232..35958232 "" http://www.snpedia.com/index.php?title=Rs10029345 reference = Chr4 illumina rs10033464 111940210..111940210 "Two SNPs from chromosome 4q25, rs2200733 and rs10033464, were found to be associated with atrial fib..." http://www.snpedia.com/index.php?title=Rs10033464 reference = Chr11 illumina rs1003483 2124119..2124119 "" http://www.snpedia.com/index.php?title=Rs1003483 reference = Chr11 snp rs1003484 2124194..2124194 "" http://www.snpedia.com/index.php?title=Rs1003484 reference = Chr15 illumina rs10046 49290278..49290278 "rs10046 is a SNP potentially linked in a gender-specific manner to hypertension" http://www.snpedia.com/index.php?title=Rs10046 reference = Chr1 illumina rs1004819 67442801..67442801 "SNP rs1004819, in the IL23R gene, is associated with increased risk for Crohn's disease in both Jewi..." http://www.snpedia.com/index.php?title=Rs1004819 reference = ChrY snp rs1005041 7630822..7630822 "" http://www.snpedia.com/index.php?title=Rs1005041 reference = Chr5 both rs10050860 96147966..96147966 "rs10050860 is one of several SNPs in the ARTS1 gene that has been shown in a large (over 1,000 Cauca..." http://www.snpedia.com/index.php?title=Rs10050860 reference = Chr5 affy rs10062446 132068273..132068273 "rs10062446 is one of two SNPs in the IL4 gene that is (somewhat) associated with penicillin allergy,..." http://www.snpedia.com/index.php?title=Rs10062446 reference = Chr12 affy rs1006737 2215556..2215556 "[http://spittoon.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-..." http://www.snpedia.com/index.php?title=Rs1006737 reference = Chr19 illumina rs1007160 38044901..38044901 "" http://www.snpedia.com/index.php?title=Rs1007160 reference = Chr2 snp rs1007371 80406856..80406856 "having minor alleles at all 3 of rs1446109-rs1007371-rs723524 may affect left-right asymmetrical bra..." http://www.snpedia.com/index.php?title=Rs1007371 reference = Chr22 illumina rs1007888 22571101..22571101 "rs1007888(C;C) was associated with an increased risk of type-2 diabetes in women [hazard ratio (95% ..." http://www.snpedia.com/index.php?title=Rs1007888 reference = Chr8 illumina rs10086908 128081119..128081119 "rs10086908 is a SNP in the 8q24 chromosomal region, which has been linked in several studies to pros..." http://www.snpedia.com/index.php?title=Rs10086908 reference = Chr8 illumina rs10087163 78058420..78058420 "" http://www.snpedia.com/index.php?title=Rs10087163 reference = Chr15 snp rs1008805 49336891..49336891 "the presence of at least one G allele at rs1008805 was significantly associated with an increase in ..." http://www.snpedia.com/index.php?title=Rs1008805 reference = Chr8 snp rs10090154 128601319..128601319 "rs10090154 is a SNP in chromosome 8q24 'region 1', associated with increased risk for prostate cance..." http://www.snpedia.com/index.php?title=Rs10090154 reference = Chr2 both rs1010 85662493..85662493 "This SNP, located on chromosome 2 in a gene (VAMP8) associated with platelet activation, may be asso..." http://www.snpedia.com/index.php?title=Rs1010 reference = Chr8 illumina rs10103355 17963214..17963214 "" http://www.snpedia.com/index.php?title=Rs10103355 reference = Chr8 snp rs10109700 128555146..128555146 "seems to have a microrna snp near 8q24 rs10109700 rs7832031" http://www.snpedia.com/index.php?title=Rs10109700 reference = Chr9 illumina rs10116277 22071397..22071397 "discussed in this [http://suicyte.wordpress.com/2007/05/26/soul-searching-i/ blog post] A region of ..." http://www.snpedia.com/index.php?title=Rs10116277 reference = Chr12 illumina rs1012672 12176182..12176182 "rs1012672 increases susceptibility to Alzheimer's disease, late-onset 1.54 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs1012672 reference = Chr1 both rs1013579 57195072..57195072 "" http://www.snpedia.com/index.php?title=Rs1013579 reference = Chr14 snp rs10151259 20859880..20859880 "[omim:CONE-ROD DYSTROPHY 9]" http://www.snpedia.com/index.php?title=Rs10151259 reference = Chr20 both rs1015362 32202273..32202273 "rs1015362 is a SNP near the ASIP (agouti signaling protein) gene on chromosome 20. This SNP is one o..." http://www.snpedia.com/index.php?title=Rs1015362 reference = Chr7 snp rs1015537 26149346..26149346 "" http://www.snpedia.com/index.php?title=Rs1015537 reference = Chr13 affy rs10162244 53784106..53784106 "" http://www.snpedia.com/index.php?title=Rs10162244 reference = Chr8 illumina rs1016343 128162479..128162479 "[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-g..." http://www.snpedia.com/index.php?title=Rs1016343 reference = Chr2 illumina rs10178458 227819679..227819679 "" http://www.snpedia.com/index.php?title=Rs10178458 reference = Chr6 snp rs1018381 15765049..15765049 "[http://originsgenomeresources.net/musings/?p=85 blog] In a population of healthy individuals, those..." http://www.snpedia.com/index.php?title=Rs1018381 reference = Chr2 snp rs10192566 11807879..11807879 "A total of 262 Korean type-2 diabetes patients were treated with 12 weeks of rosiglitazone at 4mg/da..." http://www.snpedia.com/index.php?title=Rs10192566 reference = Chr2 affy rs10200894 228525376..228525376 "rs10200894 increases susceptibility to Parkinson's disease 1.84 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs10200894 reference = Chr2 both rs10210302 233823578..233823578 "rs10210302 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs10210302 reference = Chr7 illumina rs10227893 114057313..114057313 "variations in rs17137124 and rs10227893 may impair speech" http://www.snpedia.com/index.php?title=Rs10227893 reference = Chr7 illumina rs10239794 153836827..153836827 "rs10239794, a SNP in the region of the DPP6 gene on chromosome 7, has been associated with the spora..." http://www.snpedia.com/index.php?title=Rs10239794 reference = Chr17 both rs1024611 29603901..29603901 "rs1024611, also known as the -2578A>G SNP due to its position in the promoter of the monocyte chemoa..." http://www.snpedia.com/index.php?title=Rs1024611 reference = Chr7 illumina rs10246939 141319073..141319073 "rs10246939 is one of three SNPs that form the main haplotypes behind the ability to perceive as bitt..." http://www.snpedia.com/index.php?title=Rs10246939 reference = Chr7 illumina rs10248420 87002922..87002922 "rs10248420 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tr..." http://www.snpedia.com/index.php?title=Rs10248420 reference = Chr7 snp rs10250779 44071421..44071421 "Several African-American rs10250779(T;T) homozygotes (as oriented in dbSNP) have been reported to ex..." http://www.snpedia.com/index.php?title=Rs10250779 reference = Chr7 illumina rs10258719 138106528..138106528 "" http://www.snpedia.com/index.php?title=Rs10258719 reference = Chr7 illumina rs10260404 153841731..153841731 "rs10260404, a SNP in the region of the DPP6 gene on chromosome 7, has been associated with the spora..." http://www.snpedia.com/index.php?title=Rs10260404 reference = Chr15 affy rs1026732 65882139..65882139 "rs1026732, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of rest..." http://www.snpedia.com/index.php?title=Rs1026732 reference = Chr7 illumina rs10272438 33205359..33205359 "analysis of a published data set on age related macular degeneration revealed an unreported haplotyp..." http://www.snpedia.com/index.php?title=Rs10272438 reference = Chr12 snp rs1027615 41998556..41998556 "This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients." http://www.snpedia.com/index.php?title=Rs1027615 reference = Chr7 snp rs10282312 142727929..142727929 "" http://www.snpedia.com/index.php?title=Rs10282312 reference = Chr16 snp rs1030868 54074268..54074268 "association of the MMP-2 gene with the development of lacunar stroke. rs1030868, rs2241145, rs228707..." http://www.snpedia.com/index.php?title=Rs1030868 reference = ChrX snp rs1034428 122264729..122264729 "Female carriers of an rs1034428(T) allele (as oriented in dbSNP) have a 2.19x higher risk for schizo..." http://www.snpedia.com/index.php?title=Rs1034428 reference = Chr9 illumina rs103612 133009913..133009913 "" http://www.snpedia.com/index.php?title=Rs103612 reference = Chr5 illumina rs10380 7950191..7950191 "pancreatic carcer 702 cases and 785 controls *rs162049 P = .0018; OR, 1.33; 95% CI: 1.11-1.60 *rs103..." http://www.snpedia.com/index.php?title=Rs10380 reference = Chr6 both rs1038304 151974868..151974868 "rs1038304 increases susceptibility to Bone mineral density variations, lower for carriers of the G a..." http://www.snpedia.com/index.php?title=Rs1038304 reference = Chr1 illumina rs10399805 201422621..201422621 "schizophrenia *375 case and 812 control subjects *rs10399805 p = .018 and rs2275351; p = .008." http://www.snpedia.com/index.php?title=Rs10399805 reference = Chr19 illumina rs10407022 2200477..2200477 "" http://www.snpedia.com/index.php?title=Rs10407022 reference = Chr14 snp rs1040835 92346407..92346407 "" http://www.snpedia.com/index.php?title=Rs1040835 reference = Chr10 affy rs1041296 131893021..131893021 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0030120...." http://www.snpedia.com/index.php?title=Rs1041296 reference = Chr19 snp rs10417628 2202817..2202817 "" http://www.snpedia.com/index.php?title=Rs10417628 reference = Chr18 both rs1041951 53391503..53391503 "" http://www.snpedia.com/index.php?title=Rs1041951 reference = Chr6 illumina rs1041981 31648763..31648763 "827 males and 709 females, 606 subjects without cancer and 930 subjects with various cancers *rs1041..." http://www.snpedia.com/index.php?title=Rs1041981 reference = Chr8 illumina rs1041983 18302075..18302075 "rs1041983 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1041983 reference = Chr2 illumina rs1042031 21079258..21079258 "" http://www.snpedia.com/index.php?title=Rs1042031 reference = Chr2 illumina rs1042034 21078786..21078786 "" http://www.snpedia.com/index.php?title=Rs1042034 reference = Chr1 illumina rs1042114 29011562..29011562 "rs1042114 increases susceptibility to Substance dependence, Opioid 3.56 times for carriers of the G ..." http://www.snpedia.com/index.php?title=Rs1042114 reference = Chr17 snp rs1042393 75694192..75694192 "" http://www.snpedia.com/index.php?title=Rs1042393 reference = Chr17 illumina rs1042522 7520197..7520197 "This SNP, a variant in the TP53 gene, is 1 of 25 SNPs reported to represent independently minor, but..." http://www.snpedia.com/index.php?title=Rs1042522 reference = Chr20 both rs1042523 55571213..55571213 "rs1042523 is in linkage disequilibrium with a polymorphism that increases susceptibility to Type II ..." http://www.snpedia.com/index.php?title=Rs1042523 reference = Chr20 snp rs1042579 22976724..22976724 "" http://www.snpedia.com/index.php?title=Rs1042579 reference = Chr20 illumina rs1042580 22975621..22975621 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0030120...." http://www.snpedia.com/index.php?title=Rs1042580 reference = Chr11 both rs1042602 88551344..88551344 "[omim:TYROSINASE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1042602 reference = Chr3 illumina rs1042636 123486459..123486459 "" http://www.snpedia.com/index.php?title=Rs1042636 reference = Chr8 illumina rs1042638 81112501..81112501 "rs1042638 was significantly associated with an increased risk of breast cancer" http://www.snpedia.com/index.php?title=Rs1042638 reference = Chr5 illumina rs1042713 148186633..148186633 "" http://www.snpedia.com/index.php?title=Rs1042713 reference = Chr5 snp rs1042714 148186666..148186666 "Several susceptibilities have been linked to rs1042714, a SNP in the ADRB2 gene that is also known a..." http://www.snpedia.com/index.php?title=Rs1042714 reference = Chr12 both rs1042725 64644614..64644614 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng2121.html nature] SNP rs1042725 is associated ..." http://www.snpedia.com/index.php?title=Rs1042725 reference = Chr11 illumina rs1042838 100438622..100438622 "Two SNPs in haplotype block 4 of the PGR gene were associated with an increased risk of ovarian canc..." http://www.snpedia.com/index.php?title=Rs1042838 reference = Chr21 illumina rs1042917 46370196..46370196 "" http://www.snpedia.com/index.php?title=Rs1042917 reference = Chr1 both rs1043424 20849587..20849587 "" http://www.snpedia.com/index.php?title=Rs1043424 reference = Chr19 snp rs1043994 15163844..15163844 "A study of ~100 German patients suffering from migraines reported SNP rs1043994 to be significantly ..." http://www.snpedia.com/index.php?title=Rs1043994 reference = Chr20 illumina rs1044396 61451578..61451578 "associated with vulnerability to nicotine addiction in men. [http://originsgenomeresources.net/musin..." http://www.snpedia.com/index.php?title=Rs1044396 reference = Chr12 both rs1044471 1767217..1767217 "g.-7309A>G (rs75172865) associated with lower insulin resistance and reduced the promoter activity.g..." http://www.snpedia.com/index.php?title=Rs1044471 reference = Chr6 illumina rs1044498 132214061..132214061 "[http://yannklimentidis.blogspot.com/2008/02/snps-that-may-have-made-human.html blog] ENPP1 harbors ..." http://www.snpedia.com/index.php?title=Rs1044498 reference = Chr2 snp rs1045485 201857834..201857834 "also known as D302H [PMID 15601643, PMID 17018785, PMID 17293864] Several large studies indicate tha..." http://www.snpedia.com/index.php?title=Rs1045485 reference = Chr6 snp rs10456399 32085767..32085767 "" http://www.snpedia.com/index.php?title=Rs10456399 reference = Chr7 illumina rs1045642 86976581..86976581 "rs1045642, also known as C3435T, is a SNP located in the ABCB1 gene. It is often studied in conjunct..." http://www.snpedia.com/index.php?title=Rs1045642 reference = Chr14 affy rs1045644 30424847..30424847 "" http://www.snpedia.com/index.php?title=Rs1045644 reference = Chr2 illumina rs1046974 233920286..233920286 "" http://www.snpedia.com/index.php?title=Rs1046974 reference = Chr19 snp rs1047286 6664262..6664262 "[omim:C3 POLYMORPHISM, HAV 4-1 PLUS/MINUS TYPE]" http://www.snpedia.com/index.php?title=Rs1047286 reference = Chr2 snp rs1047883 211164882..211164882 "" http://www.snpedia.com/index.php?title=Rs1047883 reference = Chr20 both rs1047972 54394870..54394870 "influences mitosis associated with cancer * breast cancer * colorectal cancer * gastric cancer" http://www.snpedia.com/index.php?title=Rs1047972 reference = Chr11 illumina rs1048047 2881186..2881186 "" http://www.snpedia.com/index.php?title=Rs1048047 reference = Chr2 snp rs1048108 215382469..215382469 "" http://www.snpedia.com/index.php?title=Rs1048108 reference = Chr5 snp rs10482605 142763714..142763714 "rs10482605(C) and rs6198 form a haplotype responsible for both regulation of glucocorticoid expressi..." http://www.snpedia.com/index.php?title=Rs10482605 reference = Chr6 illumina rs10484554 31382534..31382534 "rs10484554 was the most highly significant SNP associated with risk for psoriasis in a large US/UK s..." http://www.snpedia.com/index.php?title=Rs10484554 reference = Chr6 snp rs10485057 154454948..154454948 "rs10485057 is a SNP in the opioid receptor, mu 1 OPRM1 gene. A study of 688 Caucasian smokers (and n..." http://www.snpedia.com/index.php?title=Rs10485057 reference = Chr7 illumina rs10486567 27943088..27943088 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.91.html nature] identifies rs10486567 rs10993..." http://www.snpedia.com/index.php?title=Rs10486567 reference = Chr15 snp rs1048661 72006599..72006599 "rs1048661, also known as R141L, a SNP causing an amino acid change in the lysyl oxidase 1 LOXL1 gene..." http://www.snpedia.com/index.php?title=Rs1048661 reference = Chr7 illumina rs10488631 128381419..128381419 "rs10488631, a SNP located 3' of the IRF5 gene, has been reported as a possibly causative SNP for sys..." http://www.snpedia.com/index.php?title=Rs10488631 reference = Chr1 affy rs10489535 6266412..6266412 "rs10489535, a SNP in the ACOT7 gene, has been associated with both cholesterol levels and triglyceri..." http://www.snpedia.com/index.php?title=Rs10489535 reference = Chr1 both rs10489629 67460937..67460937 "rs10489629 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Cauca..." http://www.snpedia.com/index.php?title=Rs10489629 reference = Chr14 snp rs1048990 34831426..34831426 "rs1048990, also known as the exon-1 -8C/G SNP in the PSMA6 gene, has been reported in a large study ..." http://www.snpedia.com/index.php?title=Rs1048990 reference = Chr2 illumina rs10490162 51101161..51101161 "rs10490162 increases susceptibility to Substance dependence, Nicotine 1.65 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs10490162 reference = Chr10 affy rs10490924 124204438..124204438 "rs10490924 was identified as a risk factor from chromosome 10 related to age related macular degener..." http://www.snpedia.com/index.php?title=Rs10490924 reference = Chr12 snp rs1049174 10416632..10416632 "High- and low-natural killer (NK) activity levels have been associated with haplotypes of the KLRK1 ..." http://www.snpedia.com/index.php?title=Rs1049174 reference = Chr13 both rs10492519 50722329..50722329 "rs10492519 is one of seven SNPs found in a combined study of over 1,000 patients to be associated wi..." http://www.snpedia.com/index.php?title=Rs10492519 reference = Chr1 affy rs10493256 59461536..59461536 "rs10493256 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have ..." http://www.snpedia.com/index.php?title=Rs10493256 reference = Chr10 snp rs1049331 124211260..124211260 "*rs11200638 1.7x10-14 (-625G>A)is the most significant associated SNP with a high OR of 7.6 (95%CI: ..." http://www.snpedia.com/index.php?title=Rs1049331 reference = Chr6 both rs1049353 88910354..88910354 "Based on a study of 256 Caucasian patients being treated for depression, carriers of a rs1049353(G) ..." http://www.snpedia.com/index.php?title=Rs1049353 reference = Chr7 snp rs1049402 30601186..30601186 "" http://www.snpedia.com/index.php?title=Rs1049402 reference = Chr1 affy rs1049434 113258069..113258069 "" http://www.snpedia.com/index.php?title=Rs1049434 reference = Chr1 illumina rs10494366 160352309..160352309 "rs10494366, a SNP in the NOS1AP gene encoding the nitric oxide synthase I protein, accounts for some..." http://www.snpedia.com/index.php?title=Rs10494366 reference = Chr10 illumina rs1049550 81916682..81916682 "499 German individuals with sarcoidosis and 490 controls; Validation in an independent sample 1,649 ..." http://www.snpedia.com/index.php?title=Rs1049550 reference = Chr2 snp rs10495584 11877434..11877434 "The minor (G) allele of SNP rs10495584 was associated with lower mean systolic and diastolic blood p..." http://www.snpedia.com/index.php?title=Rs10495584 reference = Chr14 illumina rs1049564 20010446..20010446 "[omim:NUCLEOSIDE PHOSPHORYLASE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1049564 reference = Chr6 illumina rs1049623 30972808..30972808 "schizophrenia rs1049623 associated with schizophrenia (odds ratio=1.44, 95% confidence interval: 1.1..." http://www.snpedia.com/index.php?title=Rs1049623 reference = Chr2 illumina rs10498091 221607688..221607688 "Left ventricle mass, rs10498091 (p = 5.68*10(-6));" http://www.snpedia.com/index.php?title=Rs10498091 reference = Chr14 snp rs10498345 38090256..38090256 "rs10498345 is a SNP on chromosome 14 that has been associated with coronary spasm (often a precursor..." http://www.snpedia.com/index.php?title=Rs10498345 reference = Chr6 affy rs10498760 45471774..45471774 "rs10498760 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mi..." http://www.snpedia.com/index.php?title=Rs10498760 reference = Chr6 snp rs10499194 138044330..138044330 "rs10499194 associated with rheumatoid arthritis In a concurrent study, the Wellcome Trust Case Contr..." http://www.snpedia.com/index.php?title=Rs10499194 reference = Chr11 snp rs10500641 5426152..5426152 "Associated with type-2 diabetes in a Mexican-American population." http://www.snpedia.com/index.php?title=Rs10500641 reference = ChrX snp rs1050086 105086624..105086624 "[omim:THYROXINE-BINDING GLOBULIN, SLOW]" http://www.snpedia.com/index.php?title=Rs1050086 reference = Chr5 illumina rs1050152 131665208..131665208 "rs1050152, a SNP in the SLC22A4 gene known as L503F, has been associated with an autoimmune disease,..." http://www.snpedia.com/index.php?title=Rs1050152 reference = Chr11 both rs1050239 6372039..6372039 "" http://www.snpedia.com/index.php?title=Rs1050239 reference = Chr12 illumina rs1050283 10203556..10203556 "rs1050283, a SNP also known as +1073, is located in the 3' untranslated region of the oxidized low d..." http://www.snpedia.com/index.php?title=Rs1050283 reference = Chr8 illumina rs10503929 32733525..32733525 "" http://www.snpedia.com/index.php?title=Rs10503929 reference = Chr8 illumina rs10504543 73941196..73941196 "Left ventricle systolic dimension, rs10504543 (KCNB2, p = 5.18*10(-6))" http://www.snpedia.com/index.php?title=Rs10504543 reference = Chr8 affy rs10505477 128476625..128476625 "Associated with risk of colorectal cancer; (P = 0.005)" http://www.snpedia.com/index.php?title=Rs10505477 reference = Chr8 both rs10505483 128194377..128194377 "Associated with prostate cancer [http://www.biomedcentral.com/1471-2350/8/S1/S6/table/T4 table]" http://www.snpedia.com/index.php?title=Rs10505483 reference = Chr17 both rs1050565 25600202..25600202 "Testicular cancer patients may be treated with bleomycin, a cytotoxic drug that is essential compone..." http://www.snpedia.com/index.php?title=Rs1050565 reference = Chr13 affy rs10507391 30210096..30210096 "rs10507391, also known as SG13S114, is an ALOX5AP gene SNP that has been defined as part of a haplot..." http://www.snpedia.com/index.php?title=Rs10507391 reference = Chr10 illumina rs10508266 3830014..3830014 "rs10508266 and rs3750861 near KLF6 shows significant association with Lung cancer risk." http://www.snpedia.com/index.php?title=Rs10508266 reference = ChrX both rs1050828 153417411..153417411 "[omim:G6PD ASAHI]" http://www.snpedia.com/index.php?title=Rs1050828 reference = ChrX snp rs1050829 153416686..153416686 "[omim:G6PD A+]" http://www.snpedia.com/index.php?title=Rs1050829 reference = Chr10 both rs10509305 70315382..70315382 "" http://www.snpedia.com/index.php?title=Rs10509305 reference = Chr3 both rs10510468 16913627..16913627 "SNP rs10510468 has been associated with both very-low density lipoprotein levels and high-density li..." http://www.snpedia.com/index.php?title=Rs10510468 reference = Chr5 both rs10512734 40429362..40429362 "rs10512734 increases susceptibility to Crohn's disease 1.63 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs10512734 reference = Chr5 affy rs10515860 162850286..162850286 "[http://cancergenetics.wordpress.com/2007/10/13/exciting-discoveries-of-2007-breast-cancer/ cancerge..." http://www.snpedia.com/index.php?title=Rs10515860 reference = Chr4 both rs10516487 102970099..102970099 "rs17266594 rs10516487 rs3733197 gene associated with systemic lupus erythematosus." http://www.snpedia.com/index.php?title=Rs10516487 reference = Chr15 illumina rs1051730 76681394..76681394 "rs1051730, also known as D398N, is a SNP in the nicotinic acetylcholine receptor alpha 3 subunit CHR..." http://www.snpedia.com/index.php?title=Rs1051730 reference = Chr1 illumina rs1051740 224086256..224086256 "[omim:LYMPHOPROLIFERATIVE DISORDERS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1051740 reference = Chr15 affy rs10519262 48219786..48219786 "rs10519262, a intergenic SNP on chromosome 15, is reported to influence the risk for Alzheimer's dis..." http://www.snpedia.com/index.php?title=Rs10519262 reference = Chr6 illumina rs1051931 46780902..46780902 "asthma related [omim:ASTHMA AND ATOPY, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1051931 reference = Chr11 both rs1052030 76531431..76531431 "" http://www.snpedia.com/index.php?title=Rs1052030 reference = Chr3 illumina rs1052133 9773773..9773773 "rs1052133, also known as Ser326Cys, is a SNP in the oxoguanine glycosylase 1 OGG1 gene, involved in ..." http://www.snpedia.com/index.php?title=Rs1052133 reference = Chr6 illumina rs1053049 35503596..35503596 "rs1053049, rs6902123, and rs2267668 in PPARD affect Lifestyle Intervention induced changes in overal..." http://www.snpedia.com/index.php?title=Rs1053049 reference = Chr10 illumina rs1053266 61222698..61222698 "" http://www.snpedia.com/index.php?title=Rs1053266 reference = Chr21 illumina rs1053312 46247817..46247817 "" http://www.snpedia.com/index.php?title=Rs1053312 reference = Chr19 snp rs1054486 12635208..12635208 "" http://www.snpedia.com/index.php?title=Rs1054486 reference = Chr19 illumina rs1054487 12633165..12633165 "" http://www.snpedia.com/index.php?title=Rs1054487 reference = Chr2 affy rs1056836 38151707..38151707 "In a study of 153 Hispanic Caucasians with prostate cancer the rs1056836(G;G) genotype showed decrea..." http://www.snpedia.com/index.php?title=Rs1056836 reference = Chr9 illumina rs1056899 134129722..134129722 "" http://www.snpedia.com/index.php?title=Rs1056899 reference = Chr8 illumina rs1057090 6466450..6466450 "" http://www.snpedia.com/index.php?title=Rs1057090 reference = Chr8 illumina rs1057091 6487952..6487952 "" http://www.snpedia.com/index.php?title=Rs1057091 reference = Chr6 illumina rs1057141 32926751..32926751 "[omim:PEPTIDE TRANSPORTER PSF1 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1057141 reference = Chr17 illumina rs1057335 1604403..1604403 "" http://www.snpedia.com/index.php?title=Rs1057335 reference = Chr14 illumina rs1057744 104688087..104688087 "" http://www.snpedia.com/index.php?title=Rs1057744 reference = Chr10 illumina rs1057910 96731043..96731043 "SNP rs1057910(A), located in the cytochrome p450 CYP2C9 gene, most commonly encodes the amino acid i..." http://www.snpedia.com/index.php?title=Rs1057910 reference = Chr6 both rs1058768 54294106..54294106 "" http://www.snpedia.com/index.php?title=Rs1058768 reference = Chr17 illumina rs1059476 8049056..8049056 "" http://www.snpedia.com/index.php?title=Rs1059476 reference = ChrX snp rs1059703 152932023..152932023 "The C->T (Ser532Leu, rs1059703) polymorphism of the IRAK1 gene was significantly associated with ath..." http://www.snpedia.com/index.php?title=Rs1059703 reference = Chr14 snp rs1060878 38887896..38887896 "" http://www.snpedia.com/index.php?title=Rs1060878 reference = Chr16 snp rs1061009 163298..163298 "[omim:HEMOGLOBIN BUFFALO]" http://www.snpedia.com/index.php?title=Rs1061009 reference = Chr1 illumina rs1061147 194920947..194920947 "may influence age related macular degeneration when part of the haplotype of rs1061170 rs3753394 rs8..." http://www.snpedia.com/index.php?title=Rs1061147 reference = Chr1 snp rs1061170 194925860..194925860 "rs1061170 is a SNP in the complement factor H CFH gene; it is also known as Tyr402His. This SNP may ..." http://www.snpedia.com/index.php?title=Rs1061170 reference = Chr11 snp rs1061234 5227262..5227262 "[omim:HEMOGLOBIN F (LESVOS)]" http://www.snpedia.com/index.php?title=Rs1061234 reference = Chr2 illumina rs1061305 152055225..152055225 "" http://www.snpedia.com/index.php?title=Rs1061305 reference = Chr16 both rs1061646 88333478..88333478 "breast cancer rs1061646 was associated with risk in the initial study (p=0.0052), and in the replica..." http://www.snpedia.com/index.php?title=Rs1061646 reference = Chr15 both rs1062033 49335230..49335230 "rs1062033 increases susceptibility to Osteoporosis, postmenopausal for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs1062033 reference = Chr13 illumina rs1062087 74782217..74782217 "" http://www.snpedia.com/index.php?title=Rs1062087 reference = Chr5 affy rs1063499 40991318..40991318 "" http://www.snpedia.com/index.php?title=Rs1063499 reference = Chr12 illumina rs1063856 6023795..6023795 "" http://www.snpedia.com/index.php?title=Rs1063856 reference = Chr14 illumina rs1064017 95226940..95226940 "" http://www.snpedia.com/index.php?title=Rs1064017 reference = Chr11 snp rs1064074 17476318..17476318 "" http://www.snpedia.com/index.php?title=Rs1064074 reference = Chr22 snp rs1064422 22245670..22245670 "[omim:AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs1064422 reference = Chr1 snp rs1064651 153472142..153472142 "[omim:GAUCHER DISEASE, TYPE IIIC]" http://www.snpedia.com/index.php?title=Rs1064651 reference = Chr5 illumina rs1065757 78217233..78217233 "" http://www.snpedia.com/index.php?title=Rs1065757 reference = Chr22 snp rs1065852 40856638..40856638 "The (T) form of this SNP causes an amino acid change (from proline to serine) at position 34 of the ..." http://www.snpedia.com/index.php?title=Rs1065852 reference = Chr9 illumina rs1071583 136941621..136941621 "the A allele rs2989727 was significantly increased in RA patients (67%) compared with controls (60%)..." http://www.snpedia.com/index.php?title=Rs1071583 reference = Chr9 affy rs10733648 122740600..122740600 "rs10733648 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumat..." http://www.snpedia.com/index.php?title=Rs10733648 reference = Chr1 affy rs10735781 92893695..92893695 "rs10735781 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs10735781 reference = Chr12 both rs10735810 46559162..46559162 "rs10735810 increases susceptibility to Idiopathic short stature 1.33 times for heterozygotes (AG) an..." http://www.snpedia.com/index.php?title=Rs10735810 reference = Chr11 illumina rs10742772 45893843..45893843 "" http://www.snpedia.com/index.php?title=Rs10742772 reference = Chr12 illumina rs10745623 91720553..91720553 "" http://www.snpedia.com/index.php?title=Rs10745623 reference = Chr9 affy rs10757272 22078260..22078260 "rs10757272 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (CT) and..." http://www.snpedia.com/index.php?title=Rs10757272 reference = Chr9 snp rs10757274 22086055..22086055 "rs10757274 and rs2383206 can double the risk of heart disease[http://www.sciencemag.org/cgi/content/..." http://www.snpedia.com/index.php?title=Rs10757274 reference = Chr9 snp rs10757278 22114477..22114477 "This SNP, rs10757278, is one of several clustered together in a region of chromosome 9 that has been..." http://www.snpedia.com/index.php?title=Rs10757278 reference = Chr9 illumina rs10761129 93526142..93526142 "" http://www.snpedia.com/index.php?title=Rs10761129 reference = Chr10 both rs10761659 64115570..64115570 "rs10761659 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs10761659 reference = Chr10 affy rs10763546 51206405..51206405 "rs10763546 is in linkage disequilibrium with a polymorphism that increases susceptibility to Prostat..." http://www.snpedia.com/index.php?title=Rs10763546 reference = Chr11 illumina rs1076560 112788898..112788898 "rs1076560 is located in intron 6 of the dopamine receptor D2 gene. In one study of Japanese males, r..." http://www.snpedia.com/index.php?title=Rs1076560 reference = Chr11 illumina rs10790212 117207900..117207900 "Category:is a snp associated with schizophrenia rs10790212-rs4938445-rs497768" http://www.snpedia.com/index.php?title=Rs10790212 reference = Chr1 illumina rs10798269 171576336..171576336 "One of several SNPs found in a study of ~2,5720 female patients of European ancestry to be associate..." http://www.snpedia.com/index.php?title=Rs10798269 reference = Chr1 illumina rs10801575 195119404..195119404 "[http://7thspace.com/headlines/283954/the_neincbi_dbgap_database_genotypes_and_haplotypes_that_may_p..." http://www.snpedia.com/index.php?title=Rs10801575 reference = Chr9 affy rs10811661 22124094..22124094 "rs10811661 replicated as significant for type-2 diabetes risk in 1,900 Japanese patients, with odds ..." http://www.snpedia.com/index.php?title=Rs10811661 reference = Chr9 illumina rs10817610 116228387..116228387 "" http://www.snpedia.com/index.php?title=Rs10817610 reference = Chr9 snp rs10818488 122744908..122744908 "rs10818488, a SNP located in between the C5 and TRAF1 genes, was identified as the SNP from this reg..." http://www.snpedia.com/index.php?title=Rs10818488 reference = Chr11 snp rs10835638 30208928..30208928 "rs10835638, a SNP located in the (upstream) regulatory region of the follicle stimulating hormone FS..." http://www.snpedia.com/index.php?title=Rs10835638 reference = Chr12 affy rs10845271 11035068..11035068 "rs10845271 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocard..." http://www.snpedia.com/index.php?title=Rs10845271 reference = Chr9 affy rs10868366 87889880..87889880 "rs10868366, a SNP in the GOLM1 gene, is associated with reduced risk for Alzheimer's disease in a st..." http://www.snpedia.com/index.php?title=Rs10868366 reference = Chr18 illumina rs10871777 56002743..56002743 "See rs17782313 for details." http://www.snpedia.com/index.php?title=Rs10871777 reference = Chr10 affy rs10883365 101277754..101277754 "rs10883365 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs10883365 reference = Chr10 snp rs10883421 101662331..101662331 "rs10883421 is one of 2 SNPs in the DNMBP gene that has been associated with increased risk for late-..." http://www.snpedia.com/index.php?title=Rs10883421 reference = Chr10 illumina rs10883841 104924699..104924699 "" http://www.snpedia.com/index.php?title=Rs10883841 reference = Chr10 snp rs10885406 114767714..114767714 "Considered for type-2 diabetes in context with rs7903146 rs12255372 rs10885406." http://www.snpedia.com/index.php?title=Rs10885406 reference = Chr1 illumina rs10888390 148994163..148994163 "rs10888390 was significantly associated with Apo-A1 levels in a study of obese French females." http://www.snpedia.com/index.php?title=Rs10888390 reference = Chr1 snp rs10889160 60134709..60134709 "A study of 858 cases concluded that SNPs in the intron of the CYP2J2 gene were associated with incre..." http://www.snpedia.com/index.php?title=Rs10889160 reference = Chr1 illumina rs10889677 67497708..67497708 "SNP rs10889677, in the IL23R gene, is associated with increased risk for Crohn's disease in both Jew..." http://www.snpedia.com/index.php?title=Rs10889677 reference = Chr11 affy rs10892759 120969298..120969298 "rs10892759 is among several SNPs in the SORL1 gene that show some association with increased (or dec..." http://www.snpedia.com/index.php?title=Rs10892759 reference = Chr11 snp rs10893081 123118240..123118240 "rs10893081 is a SNP in the promoter region upstream of the ZNF202 gene. This SNP is also known as -6..." http://www.snpedia.com/index.php?title=Rs10893081 reference = Chr11 both rs10896380 68438978..68438978 "" http://www.snpedia.com/index.php?title=Rs10896380 reference = Chr11 illumina rs10896449 68751243..68751243 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.91.html nature] identifies rs10486567 rs10993..." http://www.snpedia.com/index.php?title=Rs10896449 reference = Chr11 snp rs10897346 55387401..55387401 "Carriers of rs10897346(C) alleles showed a 2.6-fold increased risk (CI: 1.4-4.8) for nonresponse to ..." http://www.snpedia.com/index.php?title=Rs10897346 reference = Chr4 illumina rs10902758 638643..638643 "" http://www.snpedia.com/index.php?title=Rs10902758 reference = Chr1 illumina rs10914367 31618793..31618793 "rs6996321 significantly related to spine bone mineral density (p=0.002) and rs10914367 associated wi..." http://www.snpedia.com/index.php?title=Rs10914367 reference = Chr1 snp rs10918594 160297312..160297312 "rs10918594, a SNP in the NOS1AP gene encoding the nitric oxide synthase I protein, accounts for some..." http://www.snpedia.com/index.php?title=Rs10918594 reference = Chr5 illumina rs10941112 34040464..34040464 "" http://www.snpedia.com/index.php?title=Rs10941112 reference = Chr5 snp rs10941679 44742255..44742255 "rs4415084 and rs10941679 confer risk for estrogen receptor breast cancer (ER)-positive tumors (OR = ..." http://www.snpedia.com/index.php?title=Rs10941679 reference = Chr6 affy rs10946398 20769013..20769013 "rs10946398 increases susceptibility to Type II Diabetes 1.14 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs10946398 reference = Chr6 snp rs10949483 18230485..18230485 "" http://www.snpedia.com/index.php?title=Rs10949483 reference = Chr7 snp rs10954213 128376663..128376663 "Systemic Lupus Erythematosus rs10488631 rs2004640 rs10954213 and rs729302 Japanese 277 SLE patients ..." http://www.snpedia.com/index.php?title=Rs10954213 reference = Chr8 affy rs10955924 120122524..120122524 "rs10955924 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mi..." http://www.snpedia.com/index.php?title=Rs10955924 reference = Chr9 affy rs10975200 561085..561085 "rs11164838 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs10975200 reference = Chr9 affy rs10980705 112843006..112843006 "rs10980705, also known as -2820G/A, is a SNP upstream of the endothelial differentiation, lysophosph..." http://www.snpedia.com/index.php?title=Rs10980705 reference = Chr9 affy rs10982256 116300655..116300655 "rs10982256 has been reported in a large study to be associated with bipolar disorder. The risk allel..." http://www.snpedia.com/index.php?title=Rs10982256 reference = Chr9 affy rs10984447 121024374..121024374 "rs10984447 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs10984447 reference = Chr9 both rs10985112 122771229..122771229 "rs10985112 increases susceptibility to Rheumatoid Arthritis 1.57 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs10985112 reference = ChrNone illumina rs10987386 128456138..128456138 "" http://www.snpedia.com/index.php?title=Rs10987386 reference = Chr10 illumina rs10993994 51219502..51219502 "[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-g..." http://www.snpedia.com/index.php?title=Rs10993994 reference = Chr10 snp rs10994336 61849818..61849818 "[http://spittoon.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-..." http://www.snpedia.com/index.php?title=Rs10994336 reference = Chr10 illumina rs11014002 24604659..24604659 "" http://www.snpedia.com/index.php?title=Rs11014002 reference = Chr11 snp rs11020790 93839358..93839358 "" http://www.snpedia.com/index.php?title=Rs11020790 reference = Chr11 both rs11030104 27641093..27641093 "Alzheimer's disease risk for non ApoE4 carriers is affected by the heterozygous form of rs6265, as w..." http://www.snpedia.com/index.php?title=Rs11030104 reference = Chr11 illumina rs11037909 44212190..44212190 "rs11037909 increases susceptibility to Type II Diabetes 1.27 times for heterozygotes (CT) and 1.47 t..." http://www.snpedia.com/index.php?title=Rs11037909 reference = Chr11 snp rs11039155 47237338..47237338 "NR1H3 gene SNP associated with metabolic syndrome and thus potentially type-2 diabetes and heart dis..." http://www.snpedia.com/index.php?title=Rs11039155 reference = Chr12 illumina rs11045585 20936961..20936961 "rs12762549 and rs11045585 can be used to predict whether docetaxel will induce leukopenia/neutropeni..." http://www.snpedia.com/index.php?title=Rs11045585 reference = Chr12 both rs11052552 9747225..9747225 "rs11052552 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs11052552 reference = Chr12 snp rs11053646 10204715..10204715 "[omim:MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs11053646 reference = Chr15 both rs11073964 89344765..89344765 "" http://www.snpedia.com/index.php?title=Rs11073964 reference = Chr19 snp rs11083750 50103698..50103698 "[omim:APOE4 VARIANT]" http://www.snpedia.com/index.php?title=Rs11083750 reference = Chr19 illumina rs11083846 51899494..51899494 "[http://spittoon.23andme.com/2008/08/31/snpwatch-researchers-find-first-snps-linked-to-common-type-o..." http://www.snpedia.com/index.php?title=Rs11083846 reference = Chr19 illumina rs1110627 44686551..44686551 "" http://www.snpedia.com/index.php?title=Rs1110627 reference = Chr12 snp rs11107987 94248060..94248060 "" http://www.snpedia.com/index.php?title=Rs11107987 reference = Chr12 affy rs11110912 100566344..100566344 "rs11110912 has been reported in a large study to be associated with high blood pressure. The risk al..." http://www.snpedia.com/index.php?title=Rs11110912 reference = Chr10 both rs1111875 94452862..94452862 "rs1111875 is a SNP of the HHEX homeobox gene. In several studies, it has been associated with risk f..." http://www.snpedia.com/index.php?title=Rs1111875 reference = Chr1 illumina rs11121179 8378299..8378299 "rs11121179 (p = 0.000005 for lumbar spine low bone mineral density, one of the major risk factor for..." http://www.snpedia.com/index.php?title=Rs11121179 reference = Chr11 affy rs1113132 44209979..44209979 "rs1113132 increases susceptibility to Type II Diabetes 1.15 times for heterozygotes (CG) and 1.36 ti..." http://www.snpedia.com/index.php?title=Rs1113132 reference = Chr1 snp rs1113673 117528308..117528308 "" http://www.snpedia.com/index.php?title=Rs1113673 reference = Chr9 affy rs11145338 79016147..79016147 "rs11145338 is in linkage disequilibrium with a polymorphism that increases susceptibility to Substan..." http://www.snpedia.com/index.php?title=Rs11145338 reference = Chr16 both rs11149566 81999730..81999730 "Suspected of reproducibility problems based on [http://www.kk.org/quantifiedself/2008/05/testing-gen..." http://www.snpedia.com/index.php?title=Rs11149566 reference = Chr17 illumina rs11150843 75694264..75694264 "" http://www.snpedia.com/index.php?title=Rs11150843 reference = Chr6 affy rs11155795 151893032..151893032 "rs11155795 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mi..." http://www.snpedia.com/index.php?title=Rs11155795 reference = Chr1 both rs11162922 80344646..80344646 "rs11162922 has been reported in a large study to be associated with rheumatoid arthritis. The risk a..." http://www.snpedia.com/index.php?title=Rs11162922 reference = Chr1 affy rs11164838 93167966..93167966 "rs11164838 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs11164838 reference = Chr12 illumina rs11170164 51199935..51199935 "" http://www.snpedia.com/index.php?title=Rs11170164 reference = Chr12 both rs11171739 54756892..54756892 "rs11171739 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs11171739 reference = Chr12 snp rs11178997 70618420..70618420 "rs4570625 and rs11178997 in TPH2's regulatory region display preferential transmission [http://archp..." http://www.snpedia.com/index.php?title=Rs11178997 reference = ChrNone snp rs1118473 16225645..16225645 "" http://www.snpedia.com/index.php?title=Rs1118473 reference = Chr10 affy rs11190302 101622905..101622905 "rs11190302 increases susceptibility to Alzheimer's disease, late-onset 1.39 times for heterozygotes ..." http://www.snpedia.com/index.php?title=Rs11190302 reference = Chr10 affy rs11196205 114797037..114797037 "rs12255372, rs7903146, rs7901695 and rs11196205 associated with type-2 diabetes" http://www.snpedia.com/index.php?title=Rs11196205 reference = Chr10 illumina rs11200014 123324920..123324920 "This SNP is basically a proxy for SNP rs1219648, which represents the SNP in the FGFR2 gene with the..." http://www.snpedia.com/index.php?title=Rs11200014 reference = Chr10 snp rs11200638 124210534..124210534 "rs11200638, a SNP in the HTRA1 promoter, is associated with a 10 fold increased risk of wet age rela..." http://www.snpedia.com/index.php?title=Rs11200638 reference = Chr1 illumina rs11203366 17530121..17530121 "" http://www.snpedia.com/index.php?title=Rs11203366 reference = Chr1 both rs11203367 17530203..17530203 "rs11203367 increases susceptibility to Rheumatoid Arthritis 1.26 times for carriers of the T allele ..." http://www.snpedia.com/index.php?title=Rs11203367 reference = Chr1 both rs11209026 67478546..67478546 "A relatively rare allele at SNP rs11209026, in the IL23R gene, appears to provide a fairly strong pr..." http://www.snpedia.com/index.php?title=Rs11209026 reference = Chr1 illumina rs11209032 67512680..67512680 "rs11209032 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Cauca..." http://www.snpedia.com/index.php?title=Rs11209032 reference = Chr11 affy rs11218350 120957861..120957861 "rs11218350 is among several SNPs in the SORL1 gene that show some association with increased (or dec..." http://www.snpedia.com/index.php?title=Rs11218350 reference = Chr16 affy rs1121980 52366748..52366748 "rs1121980, a SNP in the FTO gene, showed the strongest association of several SNPs in the region wit..." http://www.snpedia.com/index.php?title=Rs1121980 reference = Chr11 affy rs11225703 102691169..102691169 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs11225703 reference = Chr11 illumina rs11231898 64415412..64415412 "" http://www.snpedia.com/index.php?title=Rs11231898 reference = Chr10 snp rs11258194 13192406..13192406 "[omim:GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs11258194 reference = Chr10 both rs11259096 14518624..14518624 "" http://www.snpedia.com/index.php?title=Rs11259096 reference = Chr17 snp rs1126690 75706000..75706000 "" http://www.snpedia.com/index.php?title=Rs1126690 reference = Chr1 snp rs1126742 47171083..47171083 "rs1126742 is a SNP in the CYP4A11 gene, which encodes an enzyme that converts arachidonic acid to 20..." http://www.snpedia.com/index.php?title=Rs1126742 reference = Chr11 snp rs1126809 88657609..88657609 "rs1126809 is a SNP in the TYR tyrosinase gene. This SNP is also known as R402Q based on the amino ac..." http://www.snpedia.com/index.php?title=Rs1126809 reference = Chr1 illumina rs1127091 152046036..152046036 "This SNP, and/or perhaps neighboring SNPs around this 230 kb linkage block of chromosome 1q, influen..." http://www.snpedia.com/index.php?title=Rs1127091 reference = Chr20 snp rs1127354 3141842..3141842 "[omim:INOSINE TRIPHOSPHATASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs1127354 reference = Chr12 illumina rs11276 14884706..14884706 "[omim:DOMBROCK BLOOD GROUP]" http://www.snpedia.com/index.php?title=Rs11276 reference = Chr7 illumina rs1128349 72735590..72735590 "" http://www.snpedia.com/index.php?title=Rs1128349 reference = Chr7 illumina rs1128503 87017537..87017537 "rs1128503 is a SNP in the transporter P-glycoprotein (P-gp) 170, encoded by the ABCB1 (also known as..." http://www.snpedia.com/index.php?title=Rs1128503 reference = Chr3 snp rs1128535 49841396..49841396 "The less common allele of rs1128535, a SNP in the TRAIP gene, may have a protective effect against t..." http://www.snpedia.com/index.php?title=Rs1128535 reference = Chr15 snp rs1129038 26030454..26030454 "rs1129038 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs1129038 reference = Chr6 illumina rs1129187 43040178..43040178 "" http://www.snpedia.com/index.php?title=Rs1129187 reference = Chr8 snp rs1129424 22982258..22982258 "" http://www.snpedia.com/index.php?title=Rs1129424 reference = Chr7 illumina rs1130495 157652672..157652672 "" http://www.snpedia.com/index.php?title=Rs1130495 reference = Chr7 illumina rs1130496 157652656..157652656 "" http://www.snpedia.com/index.php?title=Rs1130496 reference = Chr2 snp rs1130609 10180371..10180371 "" http://www.snpedia.com/index.php?title=Rs1130609 reference = Chr2 both rs1130866 85747252..85747252 "rs1130866 is a SNP altering an amino acid at position 131 of the pulmonary-associated protein B surf..." http://www.snpedia.com/index.php?title=Rs1130866 reference = Chr2 illumina rs1131296 237908031..237908031 "" http://www.snpedia.com/index.php?title=Rs1131296 reference = Chr19 both rs1133330 12633090..12633090 "" http://www.snpedia.com/index.php?title=Rs1133330 reference = Chr19 illumina rs1135062 50014584..50014584 "[omim:AUBERGER BLOOD GROUP POLYMORPHISM Au(a)/Au(b)]" http://www.snpedia.com/index.php?title=Rs1135062 reference = Chr5 snp rs1135728 133506672..133506672 "(Trp336Cys) in the HMG_box region of this gene is predicted to be deleterious by many methods (SIFT,..." http://www.snpedia.com/index.php?title=Rs1135728 reference = Chr6 snp rs1135809 32085976..32085976 "" http://www.snpedia.com/index.php?title=Rs1135809 reference = Chr8 illumina rs11362 6722809..6722809 "Heterozygotes for SNP rs11362, located in the DEFB1 gene, are reported to be at increased risk for c..." http://www.snpedia.com/index.php?title=Rs11362 reference = Chr17 both rs1136287 1620026..1620026 "rs1136287, also known as Met72Thr, is a SNP in the PEDF gene. Analysis of 86 Taiwanese Chinese patie..." http://www.snpedia.com/index.php?title=Rs1136287 reference = Chr10 snp rs1136450 81041735..81041735 "rs1136450 increases susceptibility to Idiopathic pulmonary fibrosis 6.68 times for carriers of the C..." http://www.snpedia.com/index.php?title=Rs1136450 reference = Chr11 snp rs1136743 18247435..18247435 "" http://www.snpedia.com/index.php?title=Rs1136743 reference = Chr11 snp rs1136747 18247450..18247450 "" http://www.snpedia.com/index.php?title=Rs1136747 reference = Chr1 both rs1137100 65809029..65809029 "affects glucose tolerance and insulin response [omim:LEPTIN RECEPTOR POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1137100 reference = Chr1 illumina rs1137101 65831101..65831101 "[omim:LEPTIN RECEPTOR POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1137101 reference = Chr17 affy rs1137582 71461135..71461135 "" http://www.snpedia.com/index.php?title=Rs1137582 reference = Chr14 snp rs1140952 38887779..38887779 "" http://www.snpedia.com/index.php?title=Rs1140952 reference = Chr6 illumina rs1142345 18238897..18238897 "rs1142345 is a SNP in the TPMT gene, potentially encoding a variant incapable of detoxifying byprodu..." http://www.snpedia.com/index.php?title=Rs1142345 reference = Chr19 illumina rs1142530 1339538..1339538 "" http://www.snpedia.com/index.php?title=Rs1142530 reference = Chr2 both rs1143627 113310858..113310858 "associated with ankylosing spondylitis risk of Helicobacter pylori infection. Children carrying IL1..." http://www.snpedia.com/index.php?title=Rs1143627 reference = Chr2 both rs1143634 113306861..113306861 "rs1143634 increases susceptibility to Alopecia areata 2.67 times for heterozygotes (CT) and 1.13 tim..." http://www.snpedia.com/index.php?title=Rs1143634 reference = Chr16 snp rs1143679 31184312..31184312 "Causal SNP in the ITGAM (CD11b) gene in patients with SLE who are of European or African descent;(P ..." http://www.snpedia.com/index.php?title=Rs1143679 reference = Chr19 both rs1143699 5161762..5161762 "rs1143699, rs4807015, and rs1978237 confer an increased risk of developing type-2 diabetes" http://www.snpedia.com/index.php?title=Rs1143699 reference = ChrX snp rs11461 48190402..48190402 "[omim:OAT POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs11461 reference = Chr2 snp rs11465702 102424324..102424324 "associations with schizophrenia and herpes rs11465702 with schizophrenia(P = 0.005). rs11465702 was ..." http://www.snpedia.com/index.php?title=Rs11465702 reference = Chr1 illumina rs11465804 67475114..67475114 "rs11465804 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Cauca..." http://www.snpedia.com/index.php?title=Rs11465804 reference = Chr16 snp rs11466023 3239587..3239587 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs11466023 reference = Chr16 snp rs11466024 3239469..3239469 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs11466024 reference = Chr19 snp rs11466345 46535301..46535301 "colorectal neoplasia 271 colorectal adenoma cases and 544 controls, and 535 colorectal adenocarcinom..." http://www.snpedia.com/index.php?title=Rs11466345 reference = Chr1 illumina rs1151640 245902573..245902573 "rs1151640 increases susceptibility to Myocardial Infarction 1.31 times for heterozygotes (AG) and 1...." http://www.snpedia.com/index.php?title=Rs1151640 reference = Chr10 snp rs11523871 124319700..124319700 "" http://www.snpedia.com/index.php?title=Rs11523871 reference = Chr2 illumina rs11524 11883768..11883768 "This SNP is postulated to be responsible for the lower blood pressure seen associated with SNP rs104..." http://www.snpedia.com/index.php?title=Rs11524 reference = Chr8 illumina rs11535853 134053240..134053240 "" http://www.snpedia.com/index.php?title=Rs11535853 reference = Chr17 snp rs11540652 7518263..7518263 "[omim:LI-FRAUMENI SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs11540652 reference = Chr18 illumina rs1154233 19765087..19765087 "" http://www.snpedia.com/index.php?title=Rs1154233 reference = Chr4 snp rs1154404 100228027..100228027 "linked to asthma Carrying 1 or 2 copies of the minor allele of SNP rs1154404 was associated with de..." http://www.snpedia.com/index.php?title=Rs1154404 reference = Chr12 illumina rs1154510 120779718..120779718 "" http://www.snpedia.com/index.php?title=Rs1154510 reference = Chr12 illumina rs11547328 56431698..56431698 "[omim:MELANOMA, CUTANEOUS MALIGNANT, 3]" http://www.snpedia.com/index.php?title=Rs11547328 reference = Chr1 snp rs11554290 115058052..115058052 "[omim:THYROID CARCINOMA, FOLLICULAR]" http://www.snpedia.com/index.php?title=Rs11554290 reference = Chr12 illumina rs11554421 733413..733413 "" http://www.snpedia.com/index.php?title=Rs11554421 reference = Chr12 snp rs11554495 51584849..51584849 "[omim:CIRRHOSIS, CRYPTOGENIC]" http://www.snpedia.com/index.php?title=Rs11554495 reference = Chr15 illumina rs11555096 78259581..78259581 "[omim:FUMARYLACETOACETASE PSEUDODEFICIENCY]" http://www.snpedia.com/index.php?title=Rs11555096 reference = Chr5 illumina rs11556045 74020971..74020971 "[omim:HEXB POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs11556045 reference = Chr19 snp rs11557488 11419275..11419275 "" http://www.snpedia.com/index.php?title=Rs11557488 reference = Chr1 illumina rs11558492 229474714..229474714 "" http://www.snpedia.com/index.php?title=Rs11558492 reference = Chr4 both rs11559290 159821126..159821126 "" http://www.snpedia.com/index.php?title=Rs11559290 reference = Chr18 illumina rs1156044 9092140..9092140 "rs1156044(A) was significantly associated with bipolar disorder (p = 0.013) but differed in allele (..." http://www.snpedia.com/index.php?title=Rs1156044 reference = Chr5 illumina rs11568506 131699359..131699359 "rs1800925 and/or rs11568506 related to psoriasis and/or Crohn's disease ?" http://www.snpedia.com/index.php?title=Rs11568506 reference = Chr2 snp rs11568821 242442585..242442585 "[http://jcem.endojournals.org/cgi/content/abstract/92/8/3338 Abstract] intronic snp associated with ..." http://www.snpedia.com/index.php?title=Rs11568821 reference = Chr19 snp rs11569562 6629753..6629753 "A SNP in the C3 gene, rs11569562, has been associated with increased risk for adult bronchial asthma..." http://www.snpedia.com/index.php?title=Rs11569562 reference = Chr20 illumina rs11570255 57309311..57309311 "[omim:HIRSCHSPRUNG DISEASE]" http://www.snpedia.com/index.php?title=Rs11570255 reference = Chr20 illumina rs11570351 57332862..57332862 "[omim:HIRSCHSPRUNG DISEASE]" http://www.snpedia.com/index.php?title=Rs11570351 reference = Chr2 snp rs11571316 204439334..204439334 "associated with type-1 diabetes" http://www.snpedia.com/index.php?title=Rs11571316 reference = Chr13 illumina rs11571746 31843108..31843108 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs11571746 reference = Chr13 snp rs11571747 31843172..31843172 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs11571747 reference = Chr13 snp rs11571833 31870626..31870626 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs11571833 reference = Chr1 snp rs11572325 60134290..60134290 "A study of 858 cases concluded that SNPs in the intron of the CYP2J2 gene were associated with incre..." http://www.snpedia.com/index.php?title=Rs11572325 reference = ChrNone both rs11574637 31276375..31276375 "Associated with systemic lupus erythematosus (SLE)" http://www.snpedia.com/index.php?title=Rs11574637 reference = ChrNone illumina rs11575897 2715180..2715180 "" http://www.snpedia.com/index.php?title=Rs11575897 reference = Chr1 both rs11576175 148994018..148994018 "A significant association was identified between rs11576175 and Apo-A1 and HDL-C plasma levels in a ..." http://www.snpedia.com/index.php?title=Rs11576175 reference = Chr10 affy rs11594656 6162015..6162015 "rs11594656 increases susceptibility to Type I Diabetes 1.19 times for heterozygotes (AT) and 1.38 ti..." http://www.snpedia.com/index.php?title=Rs11594656 reference = Chr12 snp rs11608363 121225738..121225738 "SNPs in the IL31 gene have been associated with nonatopic eczema. Three haplotypes comprised 94% of ..." http://www.snpedia.com/index.php?title=Rs11608363 reference = Chr12 affy rs11609582 9133890..9133890 "rs11609582 increases susceptibility to Alzheimer's disease 1.78 times for heterozygotes (AT) and 1.8..." http://www.snpedia.com/index.php?title=Rs11609582 reference = Chr12 illumina rs11614913 52671866..52671866 "miRNA sequences and non-small cell lung cancer rs11614913 SNP in hsa-mir-196a2 was associated with s..." http://www.snpedia.com/index.php?title=Rs11614913 reference = Chr14 affy rs11622475 103578829..103578829 "rs11622475 has been reported in a large study to be associated with bipolar disorder. The risk allel..." http://www.snpedia.com/index.php?title=Rs11622475 reference = Chr15 snp rs11631797 26175874..26175874 "rs11631797 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, ..." http://www.snpedia.com/index.php?title=Rs11631797 reference = Chr15 both rs11635424 65824632..65824632 "rs11635424, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of res..." http://www.snpedia.com/index.php?title=Rs11635424 reference = Chr17 both rs11649743 33149092..33149092 "prostate cancer rs4430796 and rs11649743 in multiple populations, with P = 1.7 x 10(-9)" http://www.snpedia.com/index.php?title=Rs11649743 reference = Chr17 both rs11650354 43177091..43177091 "A large study of Caucasian children has identified this SNP in the TBX21 gene (and one other, rs1694..." http://www.snpedia.com/index.php?title=Rs11650354 reference = Chr17 illumina rs11650915 36276922..36276922 "" http://www.snpedia.com/index.php?title=Rs11650915 reference = Chr19 illumina rs11666067 1340517..1340517 "" http://www.snpedia.com/index.php?title=Rs11666067 reference = Chr2 snp rs11676382 85631144..85631144 "rs11676382 was associated with a warfarin maintenance dose across all analysis methods. the effects ..." http://www.snpedia.com/index.php?title=Rs11676382 reference = Chr2 both rs11677877 227839413..227839413 "" http://www.snpedia.com/index.php?title=Rs11677877 reference = Chr12 snp rs1169288 119901033..119901033 "[omim:INSULIN RESISTANCE, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1169288 reference = Chr12 snp rs1169305 119921765..119921765 "[omim:HEPATIC ADENOMA]" http://www.snpedia.com/index.php?title=Rs1169305 reference = Chr14 snp rs11694 74021035..74021035 "[omim:NIEMANN-PICK DISEASE, TYPE C2]" http://www.snpedia.com/index.php?title=Rs11694 reference = Chr2 snp rs11695471 25311212..25311212 "829 Caucasian cases with primary epithelial ovarian cancer and 941 frequency-matched unaffected cont..." http://www.snpedia.com/index.php?title=Rs11695471 reference = Chr14 illumina rs11701 20231893..20231893 "The common form at this site in most populations is rs11701(T), and the variant form is rs11701(G). ..." http://www.snpedia.com/index.php?title=Rs11701 reference = Chr13 illumina rs1170191 41573493..41573493 "In a survey that scanned 80 genes, no SNPs with a large effect were found to be associated with bipo..." http://www.snpedia.com/index.php?title=Rs1170191 reference = Chr1 snp rs1171381 188572965..188572965 "rs1171381, a SNP in the FAM5C gene, has been associated with both high-density lipoprotein levels an..." http://www.snpedia.com/index.php?title=Rs1171381 reference = Chr4 illumina rs11723091 69088065..69088065 "Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable...." http://www.snpedia.com/index.php?title=Rs11723091 reference = Chr4 snp rs11737074 125300823..125300823 "rs11737074 increases susceptibility to Parkinson's disease 1.50 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs11737074 reference = Chr5 affy rs11739135 131761296..131761296 "rs11739135 is reported to confer susceptibility to Crohn's disease." http://www.snpedia.com/index.php?title=Rs11739135 reference = Chr5 snp rs11740584 132074688..132074688 "rs11740584 is one of two SNPs in the IL4 gene that is (somewhat) associated with penicillin allergy,..." http://www.snpedia.com/index.php?title=Rs11740584 reference = Chr5 snp rs11743803 131340137..131340137 "[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16..." http://www.snpedia.com/index.php?title=Rs11743803 reference = Chr3 both rs1175543 12441433..12441433 "Associated with baseline cholesterol levels in a study of 9,000+ individuals in Washington County, M..." http://www.snpedia.com/index.php?title=Rs1175543 reference = Chr6 illumina rs11756977 56528497..56528497 "" http://www.snpedia.com/index.php?title=Rs11756977 reference = Chr6 illumina rs11758339 56435808..56435808 "" http://www.snpedia.com/index.php?title=Rs11758339 reference = Chr7 both rs11761231 131020579..131020579 "rs11761231 has been reported in a large study to be associated with rheumatoid arthritis. The risk a..." http://www.snpedia.com/index.php?title=Rs11761231 reference = Chr1 snp rs11802316 98344845..98344845 "" http://www.snpedia.com/index.php?title=Rs11802316 reference = Chr1 affy rs11805303 67448104..67448104 "rs11805303 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs11805303 reference = Chr12 snp rs11836796 87010642..87010642 "" http://www.snpedia.com/index.php?title=Rs11836796 reference = Chr14 affy rs11844707 100580366..100580366 "" http://www.snpedia.com/index.php?title=Rs11844707 reference = Chr15 illumina rs11858113 38701469..38701469 "" http://www.snpedia.com/index.php?title=Rs11858113 reference = Chr17 illumina rs11868035 17655826..17655826 "rs11868035 is one of several SNPs associated with the SREBF1 gene that show a modest association wit..." http://www.snpedia.com/index.php?title=Rs11868035 reference = Chr19 snp rs11881940 46500272..46500272 "This SNP, located in an intron of a gene (HNRPUL1) on chromosome 19, may be associated with early on..." http://www.snpedia.com/index.php?title=Rs11881940 reference = Chr2 illumina rs11886047 43704094..43704094 "rs11886047 diabetic nephropathy in 112 cases and 148 controls rs1368086 and rs725238" http://www.snpedia.com/index.php?title=Rs11886047 reference = Chr2 illumina rs11887120 25339239..25339239 "829 Caucasian cases with primary epithelial ovarian cancer and 941 frequency-matched unaffected cont..." http://www.snpedia.com/index.php?title=Rs11887120 reference = Chr2 snp rs11887534 43919751..43919751 "rs11887534, a SNP in the hepatic cholesterol transporter ABCG8 gene, has been implicated in gallston..." http://www.snpedia.com/index.php?title=Rs11887534 reference = Chr2 illumina rs11895564 173048054..173048054 "" http://www.snpedia.com/index.php?title=Rs11895564 reference = Chr2 illumina rs11898505 54538061..54538061 "rs11898505 increases susceptibility to Osteoporotic fractures for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs11898505 reference = Chr4 snp rs11934801 986555..986555 "[omim:HURLER SYNDROME]" http://www.snpedia.com/index.php?title=Rs11934801 reference = ChrNone illumina rs11938019 69107957..69107957 "Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable...." http://www.snpedia.com/index.php?title=Rs11938019 reference = Chr5 snp rs11959298 134395439..134395439 "Individuals homozygous or heterozygous for the rs11959298(A)-rs6596189(C) haplotype risk allele were..." http://www.snpedia.com/index.php?title=Rs11959298 reference = Chr6 both rs11964281 152163135..152163135 "577 African American individuals with T2DM-ESRD and 596 AA controls. *rs11964281 (nominal P = 0.0002..." http://www.snpedia.com/index.php?title=Rs11964281 reference = Chr7 both rs11971167 117069818..117069818 "[omim:VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF]" http://www.snpedia.com/index.php?title=Rs11971167 reference = Chr7 illumina rs11983225 86999456..86999456 "rs11983225 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tr..." http://www.snpedia.com/index.php?title=Rs11983225 reference = ChrX affy rs12012704 49844086..49844086 "" http://www.snpedia.com/index.php?title=Rs12012704 reference = ChrX snp rs12012834 146270673..146270673 "" http://www.snpedia.com/index.php?title=Rs12012834 reference = Chr1 illumina rs12021720 100444648..100444648 "" http://www.snpedia.com/index.php?title=Rs12021720 reference = Chr7 snp rs12026 94878952..94878952 "reports that one or two copies of a common variation (glycine replacing alanine) present at amino ac..." http://www.snpedia.com/index.php?title=Rs12026 reference = Chr1 affy rs12037606 171165025..171165025 "rs12037606 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs12037606 reference = Chr1 both rs12044852 116889302..116889302 "rs12044852 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs12044852 reference = Chr1 illumina rs1205 157948857..157948857 "Although somewhat lacking in statistical power, several reports have linked rs1205, a synonymous mut..." http://www.snpedia.com/index.php?title=Rs1205 reference = Chr1 illumina rs12075 157441978..157441978 "" http://www.snpedia.com/index.php?title=Rs12075 reference = Chr1 affy rs12079081 182520624..182520624 "rs12079081 is in linkage disequilibrium with a polymorphism that increases susceptibility to Prostat..." http://www.snpedia.com/index.php?title=Rs12079081 reference = Chr8 both rs1208 18302596..18302596 "rs1208 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an N-a..." http://www.snpedia.com/index.php?title=Rs1208 reference = Chr1 snp rs12084681 198629643..198629643 "" http://www.snpedia.com/index.php?title=Rs12084681 reference = Chr1 snp rs12094543 35589290..35589290 "rs12094543, a SNP in the ZMYM4 gene, has been reported in a large study to be associated with type-1..." http://www.snpedia.com/index.php?title=Rs12094543 reference = Chr19 illumina rs12150889 38046895..38046895 "" http://www.snpedia.com/index.php?title=Rs12150889 reference = Chr11 snp rs12184413 101894798..101894798 "rs12184413(T;T) was associated breast cancer with an odds ratio (OR) of 0.7 [95% confidence interval..." http://www.snpedia.com/index.php?title=Rs12184413 reference = Chr10 both rs1219648 123336180..123336180 "Based on a study of ~2500 female patients of European ancestry with sporadic postmenopausal breast c..." http://www.snpedia.com/index.php?title=Rs1219648 reference = Chr6 snp rs12197043 149492970..149492970 "rs12197043 and rs4897081 novel associations in type-2 diabetes patients with nephropathy from an Afr..." http://www.snpedia.com/index.php?title=Rs12197043 reference = Chr6 illumina rs12203592 341321..341321 "[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.0040004 plos] rs12203592 sh..." http://www.snpedia.com/index.php?title=Rs12203592 reference = Chr10 snp rs12248560 96511647..96511647 "rs12248560(T) defines the CYP2C19*17 allele, an ultra fast metabolizer phenotype of the CYP2C19 gene..." http://www.snpedia.com/index.php?title=Rs12248560 reference = Chr10 both rs12255372 114798892..114798892 "This SNP is in the TCF7L2 gene, and has been linked to type-2 diabetes, breast cancer and aggressive..." http://www.snpedia.com/index.php?title=Rs12255372 reference = Chr10 snp rs12268840 131215289..131215289 "Homozygous carriers of MGMT rs12268840 with frequent acid reflux had significantly higher risks of a..." http://www.snpedia.com/index.php?title=Rs12268840 reference = Chr10 snp rs12269324 131156460..131156460 "No known significant associations" http://www.snpedia.com/index.php?title=Rs12269324 reference = Chr4 snp rs1229984 100458342..100458342 "A SNP in rs1229984 encodes a form of the alcohol dehydrogenase ADH1B gene that significantly reduces..." http://www.snpedia.com/index.php?title=Rs1229984 reference = Chr6 illumina rs1230345 112489006..112489006 "" http://www.snpedia.com/index.php?title=Rs1230345 reference = Chr12 affy rs12304921 49643809..49643809 "rs12304921 has been reported in a large study to be associated with type-2 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs12304921 reference = Chr12 snp rs12316150 10203558..10203558 "rs12316150, a SNP also known as +1071, is located in the 3' untranslated region of the oxidized low ..." http://www.snpedia.com/index.php?title=Rs12316150 reference = Chr21 illumina rs12329760 41774367..41774367 "[http://7thspace.com/headlines/289665/association_of_tmprss2_erg_gene_fusion_with_clinical_character..." http://www.snpedia.com/index.php?title=Rs12329760 reference = Chr6 illumina rs1233478 29585800..29585800 "association with type 1A diabetes (rs1233478, p=1.6x10(-23), allelic odds ratio=2.0)" http://www.snpedia.com/index.php?title=Rs1233478 reference = Chr8 illumina rs12334811 48995530..48995530 "rs8178085 and rs12334811 with approaching dose-dependent effect on lung cancer predisposition, subje..." http://www.snpedia.com/index.php?title=Rs12334811 reference = Chr9 both rs12339210 116210062..116210062 "" http://www.snpedia.com/index.php?title=Rs12339210 reference = ChrNone illumina rs1236440 13842543..13842543 "" http://www.snpedia.com/index.php?title=Rs1236440 reference = Chr9 snp rs12380218 79125480..79125480 "rs12380218 increases susceptibility to Substance dependence, Nicotine 1.35 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs12380218 reference = ChrX snp rs12395818 144992415..144992415 "" http://www.snpedia.com/index.php?title=Rs12395818 reference = Chr1 illumina rs12410279 218918143..218918143 "Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a re..." http://www.snpedia.com/index.php?title=Rs12410279 reference = Chr10 snp rs12416605 29931266..29931266 "" http://www.snpedia.com/index.php?title=Rs12416605 reference = Chr11 snp rs12421995 44287885..44287885 "" http://www.snpedia.com/index.php?title=Rs12421995 reference = Chr14 illumina rs1242541 82275790..82275790 "risk of subarachnoid aneurysmal hemorrhage in Japanese population." http://www.snpedia.com/index.php?title=Rs1242541 reference = Chr14 illumina rs12434716 33338918..33338918 "" http://www.snpedia.com/index.php?title=Rs12434716 reference = Chr17 both rs12449580 6277971..6277971 "" http://www.snpedia.com/index.php?title=Rs12449580 reference = Chr2 snp rs12467557 51095774..51095774 "rs12467557 increases susceptibility to Substance dependence, Nicotine 1.81 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs12467557 reference = Chr2 illumina rs12469063 66617812..66617812 "rs12469063, a SNP located in the MEIS1 gene, has been linked to restless legs syndrome, a common sle..." http://www.snpedia.com/index.php?title=Rs12469063 reference = Chr2 snp rs12473579 202912812..202912812 "This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients." http://www.snpedia.com/index.php?title=Rs12473579 reference = Chr3 affy rs12487066 107394820..107394820 "rs12487066 has been reported in a large study to be associated with multiple sclerosis. The risk all..." http://www.snpedia.com/index.php?title=Rs12487066 reference = Chr4 snp rs12510359 169913967..169913967 "rs12510359 increases susceptibility to Myocardial Infarction 0.98 times for heterozygotes (AG) and 1..." http://www.snpedia.com/index.php?title=Rs12510359 reference = Chr8 illumina rs12544854 17973091..17973091 "" http://www.snpedia.com/index.php?title=Rs12544854 reference = Chr10 illumina rs1255372 42311786..42311786 "rs12255372, rs7903146, rs7901695 and rs11196205 associated with type-2 diabetes" http://www.snpedia.com/index.php?title=Rs1255372 reference = Chr14 snp rs1255998 63763624..63763624 "Among women rs8179176 rs9340799 rs1256065 and rs1256030 were associated with likelihood of developin..." http://www.snpedia.com/index.php?title=Rs1255998 reference = Chr14 snp rs1256030 63816923..63816923 "Among women rs8179176 rs9340799 rs1256065 and rs1256030 were associated with likelihood of developin..." http://www.snpedia.com/index.php?title=Rs1256030 reference = Chr14 illumina rs1256049 63793804..63793804 "rs2234693 rs934079 and rs1256049 variations in ESR1 gene, in addition to the age of a woman, may pre..." http://www.snpedia.com/index.php?title=Rs1256049 reference = Chr14 illumina rs1256065 63768685..63768685 "Among women rs8179176 rs9340799 rs1256065 and rs1256030 were associated with likelihood of developin..." http://www.snpedia.com/index.php?title=Rs1256065 reference = Chr15 both rs12593813 65823906..65823906 "rs12593813, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of res..." http://www.snpedia.com/index.php?title=Rs12593813 reference = Chr15 illumina rs12593929 26032853..26032853 "rs12593929 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, ..." http://www.snpedia.com/index.php?title=Rs12593929 reference = Chr15 illumina rs12594287 49311199..49311199 "The research paper suggests that the 3 snps rs17703883, rs12594287 and rs16964201 affect bone miner..." http://www.snpedia.com/index.php?title=Rs12594287 reference = Chr16 illumina rs12597511 31052720..31052720 "rs12597511, a SNP in the serine protease prostasin PRSS8 gene, has been linked to higher blood press..." http://www.snpedia.com/index.php?title=Rs12597511 reference = Chr2 illumina rs1260326 27584444..27584444 "A fine mapping approach indicates that this SNP, rs1260326, shows the strongest association signal w..." http://www.snpedia.com/index.php?title=Rs1260326 reference = Chr17 snp rs12603332 35336333..35336333 "rs12603332 is a SNP near the ORMDL3 gene, which has been linked in several studies to asthma. 264 Af..." http://www.snpedia.com/index.php?title=Rs12603332 reference = Chr2 snp rs12623467 51078593..51078593 "rs12623467 increases susceptibility to Substance dependence, Nicotine 2.09 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs12623467 reference = ChrX snp rs1263237 73488821..73488821 "" http://www.snpedia.com/index.php?title=Rs1263237 reference = Chr1 both rs1264899 111793618..111793618 "mentioned by church during bioitworld" http://www.snpedia.com/index.php?title=Rs1264899 reference = Chr8 illumina rs12674488 6325714..6325714 "" http://www.snpedia.com/index.php?title=Rs12674488 reference = ChrX snp rs12688128 103879108..103879108 "influences the risk of thyrotoxic hypokalaemic periodic paralysis rs750841 (A > T) in intron 3 of t..." http://www.snpedia.com/index.php?title=Rs12688128 reference = Chr7 snp rs12704795 94891943..94891943 "According to , variations at rs12704795, originally known as rs17876088, located in an intron of the..." http://www.snpedia.com/index.php?title=Rs12704795 reference = Chr16 affy rs12708716 11087374..11087374 "rs12708716 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs12708716 reference = Chr16 illumina rs12708965 55493820..55493820 "" http://www.snpedia.com/index.php?title=Rs12708965 reference = Chr14 snp rs1271572 63831670..63831670 "The rs1271572(T) allele was significantly more common in patients who developed MI (P < 0.001), base..." http://www.snpedia.com/index.php?title=Rs1271572 reference = Chr7 both rs12720067 87007292..87007292 "rs12720067 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tr..." http://www.snpedia.com/index.php?title=Rs12720067 reference = Chr10 affy rs12722489 6142018..6142018 "The (G) allele of rs12722489, located in the first intron of the IL2RA gene, is associated with a sl..." http://www.snpedia.com/index.php?title=Rs12722489 reference = Chr1 snp rs12722877 40545710..40545710 "" http://www.snpedia.com/index.php?title=Rs12722877 reference = Chr1 both rs12731981 43576927..43576927 "" http://www.snpedia.com/index.php?title=Rs12731981 reference = Chr1 snp rs12733102 17535292..17535292 "" http://www.snpedia.com/index.php?title=Rs12733102 reference = Chr1 snp rs12735723 159405557..159405557 "[omim:VARIEGATE PORPHYRIA, HOMOZYGOUS]" http://www.snpedia.com/index.php?title=Rs12735723 reference = Chr1 affy rs12740310 218829147..218829147 "Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a re..." http://www.snpedia.com/index.php?title=Rs12740310 reference = Chr1 both rs12749204 29048800..29048800 "rs12749204 increases susceptibility to Substance dependence, Cocaine 8.79 times for carriers of the ..." http://www.snpedia.com/index.php?title=Rs12749204 reference = Chr1 snp rs12749581 235033471..235033471 "" http://www.snpedia.com/index.php?title=Rs12749581 reference = Chr10 affy rs12762549 101610761..101610761 "rs12762549 and rs11045585 can be used to predict whether docetaxel will induced leukopenia/neutropen..." http://www.snpedia.com/index.php?title=Rs12762549 reference = Chr10 snp rs12768894 15014911..15014911 "" http://www.snpedia.com/index.php?title=Rs12768894 reference = Chr12 both rs12821256 87852466..87852466 "A 2007 study based on the Icelanders and Dutch concluded that individuals with an rs12821256(C) alle..." http://www.snpedia.com/index.php?title=Rs12821256 reference = Chr12 both rs12828016 868626..868626 "" http://www.snpedia.com/index.php?title=Rs12828016 reference = Chr14 snp rs12894182 65007642..65007642 "" http://www.snpedia.com/index.php?title=Rs12894182 reference = Chr14 illumina rs12896399 91843416..91843416 "[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000074 plos] associated wi..." http://www.snpedia.com/index.php?title=Rs12896399 reference = Chr15 illumina rs12911738 38690976..38690976 "" http://www.snpedia.com/index.php?title=Rs12911738 reference = Chr15 both rs12913832 26039213..26039213 "rs12913832 is a SNP near the OCA2 gene that may be functionally linked to blue or brown eye color, d..." http://www.snpedia.com/index.php?title=Rs12913832 reference = Chr15 illumina rs12917189 40810774..40810774 "" http://www.snpedia.com/index.php?title=Rs12917189 reference = Chr16 illumina rs12918952 76978276..76978276 "" http://www.snpedia.com/index.php?title=Rs12918952 reference = Chr16 illumina rs12918964 46289977..46289977 "" http://www.snpedia.com/index.php?title=Rs12918964 reference = Chr16 illumina rs12926089 1442858..1442858 "" http://www.snpedia.com/index.php?title=Rs12926089 reference = Chr17 snp rs12937241 37165671..37165671 "" http://www.snpedia.com/index.php?title=Rs12937241 reference = Chr17 snp rs12938245 41416446..41416446 "" http://www.snpedia.com/index.php?title=Rs12938245 reference = Chr17 snp rs12941376 30927261..30927261 "" http://www.snpedia.com/index.php?title=Rs12941376 reference = Chr17 snp rs12948217 3344452..3344452 "[omim:CANAVAN DISEASE]" http://www.snpedia.com/index.php?title=Rs12948217 reference = Chr17 both rs12951053 7518132..7518132 "rs17887200 and rs12951053 associated with ER negative breast cancer tumors (1.48 (1.11-1.93) p-trend..." http://www.snpedia.com/index.php?title=Rs12951053 reference = Chr18 illumina rs12953717 44707927..44707927 "rs12953717 is one of 3 SNPs in the SMAD7 gene associated with risk for colorectal cancer, based on a..." http://www.snpedia.com/index.php?title=Rs12953717 reference = Chr16 illumina rs12960 88147829..88147829 "" http://www.snpedia.com/index.php?title=Rs12960 reference = Chr18 both rs12970134 56035730..56035730 "A study of 14,000 Indian Asian or Caucasian adults indicates that rs12970134(A) alleles are associat..." http://www.snpedia.com/index.php?title=Rs12970134 reference = Chr2 snp rs13013209 152208695..152208695 "" http://www.snpedia.com/index.php?title=Rs13013209 reference = Chr14 illumina rs1303 93914596..93914596 "[omim:PI M3]" http://www.snpedia.com/index.php?title=Rs1303 reference = Chr2 illumina rs13031859 26595465..26595465 "" http://www.snpedia.com/index.php?title=Rs13031859 reference = Chr20 illumina rs13043752 32346969..32346969 "" http://www.snpedia.com/index.php?title=Rs13043752 reference = Chr2 illumina rs13045 88676238..88676238 "" http://www.snpedia.com/index.php?title=Rs13045 reference = Chr3 snp rs13073139 15660878..15660878 "[omim:BIOTINIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs13073139 reference = Chr3 illumina rs13073869 12328993..12328993 "Associated with risk of lung cancer in a Chinese population" http://www.snpedia.com/index.php?title=Rs13073869 reference = Chr3 snp rs13078881 15661697..15661697 "" http://www.snpedia.com/index.php?title=Rs13078881 reference = Chr4 illumina rs13107595 95797611..95797611 "" http://www.snpedia.com/index.php?title=Rs13107595 reference = Chr4 illumina rs13119723 123437763..123437763 "Of SNPs outside the HLA region, this SNP and one other (rs6822844) in the region of the IL21 gene sh..." http://www.snpedia.com/index.php?title=Rs13119723 reference = Chr4 both rs13146272 187357205..187357205 "[http://jama.ama-assn.org/cgi/content/short/299/11/1306 jama] deep vein thrombosis per risk allele o..." http://www.snpedia.com/index.php?title=Rs13146272 reference = Chr4 both rs13149290 146970416..146970416 "rs13149290 is one of seven SNPs found in a combined study of over 1,000 patients to be associated wi..." http://www.snpedia.com/index.php?title=Rs13149290 reference = Chr5 both rs13157656 41000609..41000609 "" http://www.snpedia.com/index.php?title=Rs13157656 reference = Chr22 illumina rs131690 21978009..21978009 "rs131690, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for bipola..." http://www.snpedia.com/index.php?title=Rs131690 reference = Chr22 illumina rs131702 21980987..21980987 "rs131702, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for bipola..." http://www.snpedia.com/index.php?title=Rs131702 reference = Chr19 illumina rs13181 50546759..50546759 "" http://www.snpedia.com/index.php?title=Rs13181 reference = Chr5 snp rs13186787 153706962..153706962 "" http://www.snpedia.com/index.php?title=Rs13186787 reference = Chr6 illumina rs13192841 138008907..138008907 "An association was found between Systemic lupus erythematosus (SLE) and rs13192841." http://www.snpedia.com/index.php?title=Rs13192841 reference = Chr6 illumina rs13194995 56578510..56578510 "" http://www.snpedia.com/index.php?title=Rs13194995 reference = Chr6 affy rs13207033 138007111..138007111 "rs13207033 can be considered a proxy for rs10499194, since it is perfectly correlated to it (r2..." http://www.snpedia.com/index.php?title=Rs13207033 reference = Chr1 affy rs1321172 66503301..66503301 "rs1321172 has been reported in a large study to be associated with multiple sclerosis. The risk alle..." http://www.snpedia.com/index.php?title=Rs1321172 reference = Chr7 snp rs13225697 7727006..7727006 "rs4568789 (chromosome 1q25) and tagSNP rs13225697 (chromosome 7p21) to be significantly associated w..." http://www.snpedia.com/index.php?title=Rs13225697 reference = Chr1 snp rs1322784 229995558..229995558 "rs1322784, an intragenic SNP associated with the 'disrupted in schizophrenia' DISC1 gene, was report..." http://www.snpedia.com/index.php?title=Rs1322784 reference = Chr13 illumina rs1324913 73533589..73533589 "Based on a study of 400 Spanish patients with rheumatoid arthritis, SNP rs1324913 in the KLF12 gene ..." http://www.snpedia.com/index.php?title=Rs1324913 reference = Chr1 illumina rs1325310 199345858..199345858 "[omim:THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1325310 reference = Chr8 snp rs13254738 128173525..128173525 "rs13254738 increases susceptibility to Prostate cancer 1.18 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs13254738 reference = Chr8 snp rs13265018 22941965..22941965 "" http://www.snpedia.com/index.php?title=Rs13265018 reference = Chr8 both rs13265557 87729216..87729216 "" http://www.snpedia.com/index.php?title=Rs13265557 reference = Chr8 illumina rs13266634 118253964..118253964 "rs13266634 is a SNP in the zinc transporter protein member 8 SLC30A8 gene that has primarily been as..." http://www.snpedia.com/index.php?title=Rs13266634 reference = Chr8 illumina rs13277113 11386595..11386595 "Associated with systemic lupus erythematosus (SLE)" http://www.snpedia.com/index.php?title=Rs13277113 reference = Chr8 snp rs13281615 128424800..128424800 "breast cancer *rs13281615 in 8q24 was stronger for ER-positive, PR-positive, and low grade tumors (P..." http://www.snpedia.com/index.php?title=Rs13281615 reference = Chr13 illumina rs1328674 46339708..46339708 "rs1328675 is part of a 4-SNP haplotype in the serotonin 2A receptor gene HTR2A that has been associa..." http://www.snpedia.com/index.php?title=Rs1328674 reference = Chr9 both rs13293564 35156763..35156763 "rs2281999 and rs13293564 (G/T) diabetic nephropathy type-1 diabetes case/control (1176/1323) study f..." http://www.snpedia.com/index.php?title=Rs13293564 reference = Chr1 illumina rs1329428 194969433..194969433 "linked to blindness in age related macular degeneration rs3753394, rs800292, rs1061147, rs1061170, r..." http://www.snpedia.com/index.php?title=Rs1329428 reference = Chr7 illumina rs13306435 22737564..22737564 "A haplotype of the IL6 gene appears to be overrepresented in sciatica patients.[PMID 15733644, PMID ..." http://www.snpedia.com/index.php?title=Rs13306435 reference = Chr17 snp rs13306487 42724787..42724787 "[omim:Ca/Tu ALLOANTIGEN POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs13306487 reference = ChrNone illumina rs13327941 69104740..69104740 "Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable...." http://www.snpedia.com/index.php?title=Rs13327941 reference = Chr9 illumina rs1333040 22073404..22073404 "A common variant on chromosome 9p21 affects the risk of myocardial infarction, and is further discus..." http://www.snpedia.com/index.php?title=Rs1333040 reference = Chr9 affy rs1333042 22093813..22093813 "rs1333042 increases susceptibility to Coronary artery disease 1.29 times for heterozygotes (AG) and ..." http://www.snpedia.com/index.php?title=Rs1333042 reference = Chr9 affy rs1333048 22115347..22115347 "rs1333048 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AC) and ..." http://www.snpedia.com/index.php?title=Rs1333048 reference = Chr9 affy rs1333049 22115503..22115503 "rs1333049 has been reported in a large study to be associated with heart disease, in particular, cor..." http://www.snpedia.com/index.php?title=Rs1333049 reference = Chr16 snp rs13336129 49733159..49733159 "" http://www.snpedia.com/index.php?title=Rs13336129 reference = Chr6 snp rs1334710 6528720..6528720 "rs1334710, a SNP purported to be in the promoter of the LY86 gene, is reported to be associated with..." http://www.snpedia.com/index.php?title=Rs1334710 reference = Chr5 affy rs13361189 150203580..150203580 "[http://spittoon.23andme.com/2008/08/25/researchers-find-biological-basis-for-crohns-association/ sp..." http://www.snpedia.com/index.php?title=Rs13361189 reference = Chr19 snp rs13382089 58911666..58911666 "" http://www.snpedia.com/index.php?title=Rs13382089 reference = Chr2 illumina rs13387042 217614077..217614077 "rs13387042(A;A) on has an estimated 1.44-fold greater risk than noncarriers," http://www.snpedia.com/index.php?title=Rs13387042 reference = Chr22 illumina rs133885 24489289..24489289 "" http://www.snpedia.com/index.php?title=Rs133885 reference = Chr2 both rs13397985 230799467..230799467 "[http://spittoon.23andme.com/2008/08/31/snpwatch-researchers-find-first-snps-linked-to-common-type-o..." http://www.snpedia.com/index.php?title=Rs13397985 reference = Chr2 snp rs13420827 25307472..25307472 "829 Caucasian cases with primary epithelial ovarian cancer and 941 frequency-matched unaffected cont..." http://www.snpedia.com/index.php?title=Rs13420827 reference = Chr1 affy rs1343125 113912559..113912559 "rs1343125, a SNP in the MAGI3 gene, was associated with rheumatoid arthritis." http://www.snpedia.com/index.php?title=Rs1343125 reference = Chr1 illumina rs1343151 67491717..67491717 "rs1343151 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Caucas..." http://www.snpedia.com/index.php?title=Rs1343151 reference = Chr16 affy rs1344484 51469800..51469800 "rs1344484 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs1344484 reference = Chr2 both rs1344706 185486673..185486673 "linked to schizophrenia" http://www.snpedia.com/index.php?title=Rs1344706 reference = ChrY snp rs13447347 21157894..21157894 "" http://www.snpedia.com/index.php?title=Rs13447347 reference = ChrY snp rs13447348 21158586..21158586 "" http://www.snpedia.com/index.php?title=Rs13447348 reference = ChrY illumina rs13447352 21159241..21159241 "" http://www.snpedia.com/index.php?title=Rs13447352 reference = ChrY illumina rs13447353 21159562..21159562 "" http://www.snpedia.com/index.php?title=Rs13447353 reference = ChrY illumina rs13447354 21160339..21160339 "" http://www.snpedia.com/index.php?title=Rs13447354 reference = ChrY illumina rs13447360 21164059..21164059 "" http://www.snpedia.com/index.php?title=Rs13447360 reference = ChrNone snp rs13447361 2881786..2881786 "" http://www.snpedia.com/index.php?title=Rs13447361 reference = ChrY snp rs13447367 20338150..20338150 "" http://www.snpedia.com/index.php?title=Rs13447367 reference = ChrY snp rs13447368 20338096..20338096 "" http://www.snpedia.com/index.php?title=Rs13447368 reference = ChrY snp rs13447369 20338213..20338213 "" http://www.snpedia.com/index.php?title=Rs13447369 reference = ChrY snp rs13447370 20223888..20223888 "" http://www.snpedia.com/index.php?title=Rs13447370 reference = ChrY snp rs13447372 21154381..21154381 "" http://www.snpedia.com/index.php?title=Rs13447372 reference = ChrNone snp rs13447373 13977179..13977179 "" http://www.snpedia.com/index.php?title=Rs13447373 reference = ChrNone snp rs13447374 13540161..13540161 "" http://www.snpedia.com/index.php?title=Rs13447374 reference = ChrNone snp rs13447375 13540272..13540272 "" http://www.snpedia.com/index.php?title=Rs13447375 reference = ChrNone illumina rs13447376 13979134..13979134 "" http://www.snpedia.com/index.php?title=Rs13447376 reference = ChrY snp rs13447377 20327106..20327106 "" http://www.snpedia.com/index.php?title=Rs13447377 reference = ChrY snp rs13447378 21151128..21151128 "" http://www.snpedia.com/index.php?title=Rs13447378 reference = ChrY snp rs13447379 21151187..21151187 "" http://www.snpedia.com/index.php?title=Rs13447379 reference = ChrY snp rs13447380 21151158..21151158 "" http://www.snpedia.com/index.php?title=Rs13447380 reference = ChrY snp rs13447442 21162467..21162467 "" http://www.snpedia.com/index.php?title=Rs13447442 reference = Chr17 snp rs13447447 58919624..58919624 "rs13447447 is one of four SNPs representing perhaps the best studied ACE SNP. It is actually not a s..." http://www.snpedia.com/index.php?title=Rs13447447 reference = Chr11 snp rs13447640 93839369..93839369 "" http://www.snpedia.com/index.php?title=Rs13447640 reference = Chr1 snp rs13551 24053549..24053549 "[omim:FU1/FU2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs13551 reference = Chr22 illumina rs135551 44931685..44931685 "667 cases and 862 controls (OR=0.87, P=0.046, 95% CI=0.72-0.99 for rs135551; OR=0.80, P=0.034, 95% m..." http://www.snpedia.com/index.php?title=Rs135551 reference = Chr15 illumina rs1355920 30145020..30145020 "associated with specific patterns of brain activity. rs3087454 rs1355920 rs7520974 rs885834" http://www.snpedia.com/index.php?title=Rs1355920 reference = Chr22 affy rs135745 37013583..37013583 "This SNP, located in the 3' UTR of the CSNK1E gene, has been associated with sensitivity to the acut..." http://www.snpedia.com/index.php?title=Rs135745 reference = Chr6 both rs1360780 35715549..35715549 "In Caucasian non-Hispanics, the rs1360780(T) allele is associated with increased risk for depression..." http://www.snpedia.com/index.php?title=Rs1360780 reference = Chr2 affy rs1368086 43818511..43818511 "rs11886047 diabetic nephropathy in 112 cases and 148 controls rs1368086 and rs725238" http://www.snpedia.com/index.php?title=Rs1368086 reference = Chr5 illumina rs1373692 40466940..40466940 "rs1373692 increases susceptibility to Crohn's disease 1.46 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs1373692 reference = Chr2 affy rs1375144 115957656..115957656 "rs1375144, a SNP in the DPP10 gene, has been reported in a large study to be associated with bipolar..." http://www.snpedia.com/index.php?title=Rs1375144 reference = Chr12 snp rs1376251 11030119..11030119 "rs1376251 increases susceptibility to Myocardial Infarction 1.23 times for heterozygotes (CT) and 1...." http://www.snpedia.com/index.php?title=Rs1376251 reference = Chr4 illumina rs1379659 20229781..20229781 "Left ventricle diastolic dimension, rs1379659 (SLIT2, p = 1.17*10(-7))" http://www.snpedia.com/index.php?title=Rs1379659 reference = Chr18 illumina rs1380866 27309955..27309955 "" http://www.snpedia.com/index.php?title=Rs1380866 reference = Chr4 illumina rs1383180 5836343..5836343 "" http://www.snpedia.com/index.php?title=Rs1383180 reference = Chr12 snp rs1386494 70638810..70638810 "an association with rs1386494 SNP was observed in the subgroup of female patients with pure PD pheno..." http://www.snpedia.com/index.php?title=Rs1386494 reference = Chr17 illumina rs1391768 8281591..8281591 "275 Caucasian schizophrenia patients and 200 controls rs1391768 imparting a significant effect but o..." http://www.snpedia.com/index.php?title=Rs1391768 reference = Chr11 both rs1393350 88650694..88650694 "rs1393350 increases susceptibility to Blond rather than brown hair 1.29 times for carriers of the A ..." http://www.snpedia.com/index.php?title=Rs1393350 reference = Chr1 illumina rs13962 157442151..157442151 "" http://www.snpedia.com/index.php?title=Rs13962 reference = Chr10 both rs1398024 23705444..23705444 "Crohn's disease and sarcoidosis 1,317 patients (660 CD and 657 SA) and 1,091 controls. rs1398024(A) ..." http://www.snpedia.com/index.php?title=Rs1398024 reference = Chr2 snp rs1401296 127905778..127905778 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0030120...." http://www.snpedia.com/index.php?title=Rs1401296 reference = Chr22 both rs140504 21957369..21957369 "rs140504, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for bipola..." http://www.snpedia.com/index.php?title=Rs140504 reference = Chr22 snp rs140523 49309648..49309648 "" http://www.snpedia.com/index.php?title=Rs140523 reference = Chr3 illumina rs140693 130638141..130638141 "We observed a significantly decreased risk of lung cancer associated with the *rs140693(A;G) genotyp..." http://www.snpedia.com/index.php?title=Rs140693 reference = Chr17 both rs140701 25562658..25562658 "A study of patients with panic disorder or social anxiety disorder, both moderately heritable anxiet..." http://www.snpedia.com/index.php?title=Rs140701 reference = Chr1 illumina rs1411771 230241398..230241398 "13 single-nucleotide polymorphisms (SNPs) in 723 members of 179 Finnish Bipolar disorder families. *..." http://www.snpedia.com/index.php?title=Rs1411771 reference = Chr16 both rs1421085 52358455..52358455 "Within the FTO gene, many SNPs appear to be co-inherited. The SNP showing the strongest association ..." http://www.snpedia.com/index.php?title=Rs1421085 reference = Chr18 both rs1426310 27152292..27152292 "" http://www.snpedia.com/index.php?title=Rs1426310 reference = Chr15 illumina rs1426654 46213776..46213776 "This SNP influences skin pigmentation. The allele p.A111T, rs1426654(A), indicates light-skinned eur..." http://www.snpedia.com/index.php?title=Rs1426654 reference = Chr20 snp rs143383 33489397..33489397 "rs143383 showed significant association with hip osteoarthritis in two independent Japanese populati..." http://www.snpedia.com/index.php?title=Rs143383 reference = Chr9 illumina rs1435252 100143412..100143412 "Associated with nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs1435252 reference = Chr15 affy rs1442295 85763691..85763691 "rs1442295 is a SNP in chromosome 8q24, region 1, associated both with overall risk for prostate canc..." http://www.snpedia.com/index.php?title=Rs1442295 reference = Chr5 illumina rs1445898 35946286..35946286 "rs1445898 is associated with some protection from type-1 diabetes in several European populations." http://www.snpedia.com/index.php?title=Rs1445898 reference = Chr2 both rs1446109 80391930..80391930 "having minor alleles at all 3 of rs1446109-rs1007371-rs723524 may affect left-right asymmetrical bra..." http://www.snpedia.com/index.php?title=Rs1446109 reference = Chr2 illumina rs1446495 116242430..116242430 "" http://www.snpedia.com/index.php?title=Rs1446495 reference = Chr8 illumina rs1447295 128554220..128554220 "rs1447295 is a SNP on chromosome 8q24, associated with increased risk for prostate cancer in several..." http://www.snpedia.com/index.php?title=Rs1447295 reference = Chr13 illumina rs144848 31804729..31804729 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs144848 reference = Chr9 illumina rs1454626 2611030..2611030 "associated with carotid artery disease, BMI, and LDL-associated apolipoprotein B" http://www.snpedia.com/index.php?title=Rs1454626 reference = Chr3 snp rs1455832 79258806..79258806 "[http://www.genengnews.com/news/bnitem.aspx?name=33143258 news] affects obesity strongest during chi..." http://www.snpedia.com/index.php?title=Rs1455832 reference = Chr1 snp rs1466731 152841444..152841444 "" http://www.snpedia.com/index.php?title=Rs1466731 reference = Chr1 snp rs1470407 59487580..59487580 "rs1470407 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have b..." http://www.snpedia.com/index.php?title=Rs1470407 reference = Chr3 both rs1470579 187011774..187011774 "rs1470579 replicated as significant for type-2 diabetes risk in 1,900 Japanese patients, with odds r..." http://www.snpedia.com/index.php?title=Rs1470579 reference = Chr5 illumina rs1494555 35906947..35906947 "[omim:SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CE..." http://www.snpedia.com/index.php?title=Rs1494555 reference = Chr5 illumina rs1494558 35896825..35896825 "[omim:SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CE..." http://www.snpedia.com/index.php?title=Rs1494558 reference = Chr12 affy rs1495377 69863368..69863368 "rs1495377 has been reported in a large study to be associated with type-2 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs1495377 reference = Chr1 illumina rs1495965 67526096..67526096 "rs1495965 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Caucas..." http://www.snpedia.com/index.php?title=Rs1495965 reference = Chr3 illumina rs1501299 188053817..188053817 "A study of 733 breast cancer cases for 10 SNPs concluded that the rs1501299(C;C) genotype (in dbSNP ..." http://www.snpedia.com/index.php?title=Rs1501299 reference = ChrY snp rs150173 23396453..23396453 "" http://www.snpedia.com/index.php?title=Rs150173 reference = Chr11 illumina rs1503185 48103198..48103198 "" http://www.snpedia.com/index.php?title=Rs1503185 reference = Chr4 snp rs1509269 138973174..138973174 "rs1509269 increases susceptibility to Parkinson's disease 1.71 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs1509269 reference = Chr10 affy rs1509957 64280724..64280724 "Associated with type-2 diabetes in a Mexican-American population." http://www.snpedia.com/index.php?title=Rs1509957 reference = Chr2 illumina rs1516446 189583666..189583666 "" http://www.snpedia.com/index.php?title=Rs1516446 reference = Chr5 illumina rs15251 149756425..149756425 "rs2255796 and rs15251 suggested excess maternal transmission and may influence risk of cleft palate" http://www.snpedia.com/index.php?title=Rs15251 reference = Chr11 illumina rs1528133 8106329..8106329 "rs1528133, a SNP in the TUB gene, was found in a study of 492 unrelated type-2 diabetes patients to ..." http://www.snpedia.com/index.php?title=Rs1528133 reference = Chr16 snp rs1529927 55462088..55462088 "" http://www.snpedia.com/index.php?title=Rs1529927 reference = Chr5 illumina rs1530498 13955220..13955220 "" http://www.snpedia.com/index.php?title=Rs1530498 reference = Chr5 illumina rs153477 150619602..150619602 "" http://www.snpedia.com/index.php?title=Rs153477 reference = Chr5 both rs153478 150619632..150619632 "" http://www.snpedia.com/index.php?title=Rs153478 reference = Chr22 both rs1534891 37025045..37025045 "Along with rs6442925 and rs534654, this SNP, rs1534891, is part of a 3-SNP (multi-locus) interaction..." http://www.snpedia.com/index.php?title=Rs1534891 reference = Chr11 illumina rs1535 61354548..61354548 "4+ IQ points for breastfeeding with the AA or AG genotypes" http://www.snpedia.com/index.php?title=Rs1535 reference = Chr6 illumina rs1535435 135798715..135798715 "Originally reported to be associated with type-2 diabetes in a genome-wide association study; yet th..." http://www.snpedia.com/index.php?title=Rs1535435 reference = Chr9 illumina rs1538660 110681646..110681646 "" http://www.snpedia.com/index.php?title=Rs1538660 reference = Chr1 affy rs1538979 229963491..229963491 "schizophrenia and bipolar disorder rs1538979 (P=0.016; odds ratio=2.73+/-95% confidence interval (CI..." http://www.snpedia.com/index.php?title=Rs1538979 reference = Chr5 illumina rs154001 127713034..127713034 "" http://www.snpedia.com/index.php?title=Rs154001 reference = Chr6 both rs1540771 411033..411033 "[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000074 plos] the associati..." http://www.snpedia.com/index.php?title=Rs1540771 reference = Chr12 both rs1544410 46526102..46526102 "rs1544410 increases susceptibility to Shorter stature for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs1544410 reference = Chr3 both rs1545985 45980482..45980482 "rs1545985 is one of seven SNPs found in a combined study of over 1,000 patients to be associated wit..." http://www.snpedia.com/index.php?title=Rs1545985 reference = Chr3 illumina rs1550922 59634698..59634698 "SNP rs1550922 has been associated with both glucose levels and body-mass index (eg obesity) in the F..." http://www.snpedia.com/index.php?title=Rs1550922 reference = Chr15 illumina rs1552311 46368005..46368005 "" http://www.snpedia.com/index.php?title=Rs1552311 reference = Chr4 snp rs1554483 56016574..56016574 "A study of 391 overweight patients concluded that the haplotype of rs1554483(G) and rs4864548(A) was..." http://www.snpedia.com/index.php?title=Rs1554483 reference = Chr9 illumina rs1554973 119520633..119520633 "In the study the researchers analysed DNA from placental tissue samples and cord blood from 111 wome..." http://www.snpedia.com/index.php?title=Rs1554973 reference = ChrY illumina rs1558843 21159971..21159971 "" http://www.snpedia.com/index.php?title=Rs1558843 reference = Chr6 affy rs1559874 32351133..32351133 "rs1559874 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone min..." http://www.snpedia.com/index.php?title=Rs1559874 reference = Chr11 both rs1566734 48101951..48101951 "[omim:COLON CANCER, SOMATIC]" http://www.snpedia.com/index.php?title=Rs1566734 reference = Chr6 both rs1569788 152370309..152370309 "577 African American individuals with T2DM-ESRD and 596 AA controls. *rs1569788 (nominal P = 0.00075..." http://www.snpedia.com/index.php?title=Rs1569788 reference = Chr6 snp rs1570360 43845808..43845808 "This position is referred to as the -1154 position in many VEGF-associated publications. The normal ..." http://www.snpedia.com/index.php?title=Rs1570360 reference = Chr9 both rs1571801 123467194..123467194 "In a study of ~1000 Caucasian patients with prostate cancer, rs1571801 was the SNP most associated w..." http://www.snpedia.com/index.php?title=Rs1571801 reference = Chr9 both rs1572983 103173449..103173449 "" http://www.snpedia.com/index.php?title=Rs1572983 reference = Chr4 illumina rs1573496 100568692..100568692 "rs1573496 is a SNP in the ADH7 alcohol dehydrogenase 7 gene. A study of over 3,800 cases of 'upper a..." http://www.snpedia.com/index.php?title=Rs1573496 reference = Chr6 snp rs15793179 20347038..20347038 "the (C;C) genotype is linked to death for chickens" http://www.snpedia.com/index.php?title=Rs15793179 reference = Chr6 snp rs1582055 131186056..131186056 "risk of cardiovascular disease rs1582055 and rs4897475 in erythrocyte membrane protein band 4.1-like..." http://www.snpedia.com/index.php?title=Rs1582055 reference = Chr9 illumina rs1590 100955986..100955986 "appears relevant to colon cancer rs334348, rs334349 and rs1590 (in total linkage disequilibrium with..." http://www.snpedia.com/index.php?title=Rs1590 reference = Chr7 snp rs1592377 126678687..126678687 "" http://www.snpedia.com/index.php?title=Rs1592377 reference = Chr19 illumina rs1613662 60228407..60228407 "[http://jama.ama-assn.org/cgi/content/short/299/11/1306 jama] deep vein thrombosis per risk allele o..." http://www.snpedia.com/index.php?title=Rs1613662 reference = Chr7 illumina rs16139 24291404..24291404 "[omim:NEUROPEPTIDE Y POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs16139 reference = Chr17 affy rs161400 3508145..3508145 "" http://www.snpedia.com/index.php?title=Rs161400 reference = Chr7 illumina rs16147 24289935..24289935 "located in the promoter region alters NPY expression in vitro and seems to account for more than hal..." http://www.snpedia.com/index.php?title=Rs16147 reference = Chr7 illumina rs1617640 100155234..100155234 "the T allele of SNP rs1617640 in the promoter of the EPO gene is significantly associated with Proli..." http://www.snpedia.com/index.php?title=Rs1617640 reference = Chr5 illumina rs162036 7938959..7938959 "" http://www.snpedia.com/index.php?title=Rs162036 reference = Chr5 snp rs162049 7946121..7946121 "Pancreatic cancer 702 cases and 785 controls *rs162049 p = .024, OR 1.33, CI: 1.11-1.60 *rs10380 (Hi..." http://www.snpedia.com/index.php?title=Rs162049 reference = Chr1 snp rs1621005 17535338..17535338 "rs1621005 increases susceptibility to Rheumatoid Arthritis 1.89 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs1621005 reference = Chr16 illumina rs16260 67328535..67328535 "[PMID 14961571, PMID 16189707] rs16260 (A) SNP located in the promoter region of the E-cadherin CDH1..." http://www.snpedia.com/index.php?title=Rs16260 reference = Chr19 both rs1640262 2730134..2730134 "Polycystic ovary syndrome PCOS. (287 cases, 187 controls) rs1640262, homozygotes for the minor allel..." http://www.snpedia.com/index.php?title=Rs1640262 reference = Chr5 illumina rs1650697 79986537..79986537 "" http://www.snpedia.com/index.php?title=Rs1650697 reference = Chr1 snp rs1655285 229766097..229766097 "13 single-nucleotide polymorphisms (SNPs) in 723 members of 179 Finnish Bipolar disorder families. *..." http://www.snpedia.com/index.php?title=Rs1655285 reference = Chr22 snp rs165599 18336781..18336781 "anxiety-related personality traits, ADHD, schizophrenia part of a three marker haplotype rs737865-rs..." http://www.snpedia.com/index.php?title=Rs165599 reference = Chr15 illumina rs1667394 26203777..26203777 "rs1667394 increases susceptibility to Blond rather than brown hair 4.94 times for carriers of the A ..." http://www.snpedia.com/index.php?title=Rs1667394 reference = Chr2 both rs1670283 29270076..29270076 "" http://www.snpedia.com/index.php?title=Rs1670283 reference = Chr1 illumina rs1676486 103126726..103126726 "Lumbar disc herniation (LDH), a form of lumbar disc disease, is one of the most common musculoskelet..." http://www.snpedia.com/index.php?title=Rs1676486 reference = Chr2 affy rs16851009 166338953..166338953 "rs16851009 increases susceptibility to Parkinson's disease 1.84 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs16851009 reference = Chr4 illumina rs16853571 41447887..41447887 "rs16853571 increases susceptibility to Crohn's disease 1.45 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs16853571 reference = Chr6 snp rs16874954 46785057..46785057 "[omim:PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs16874954 reference = Chr6 snp rs16879498 49688206..49688206 "[omim:RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE]" http://www.snpedia.com/index.php?title=Rs16879498 reference = Chr4 illumina rs16890979 9531265..9531265 "(Val253Ile; rs16890979) in GLUT9 was most strongly associated with uric acid levels, with each copy ..." http://www.snpedia.com/index.php?title=Rs16890979 reference = Chr5 illumina rs16891982 33987450..33987450 "This snp influences skin pigmentation. The allele p.L374F indicates light-skinned european ancestry ..." http://www.snpedia.com/index.php?title=Rs16891982 reference = Chr8 affy rs16901979 128194098..128194098 "rs16901979 is a SNP on chromosome 8q24, associated with increased risk for prostate cancer in severa..." http://www.snpedia.com/index.php?title=Rs16901979 reference = Chr10 snp rs16906252 131155535..131155535 "strongly associated with MGMT methylation (multivariate odds ratio 18.0; 95% confidence interval, 6...." http://www.snpedia.com/index.php?title=Rs16906252 reference = Chr4 snp rs1693482 100482988..100482988 "rs1693482, also known as Ile271Gln, is a SNP in the alcohol dehydrogenase 1C ADH1C gene. A study of ..." http://www.snpedia.com/index.php?title=Rs1693482 reference = Chr5 snp rs1694089 53283151..53283151 "" http://www.snpedia.com/index.php?title=Rs1694089 reference = Chr17 illumina rs16942 38497526..38497526 "This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs16942 reference = Chr2 illumina rs16944 113311338..113311338 "rs16944 increases susceptibility to Osteoarthritis 1.80 times for heterozygotes (AG) and 2.90 times ..." http://www.snpedia.com/index.php?title=Rs16944 reference = Chr22 snp rs16947 40853887..40853887 "The 'standard' nucleotide at this SNP is (G). The (A) variant causes an amino acid change (from argi..." http://www.snpedia.com/index.php?title=Rs16947 reference = Chr17 both rs16947078 43180499..43180499 "A large study of Caucasian children has identified this SNP in the TBX21 gene (and one other, rs1165..." http://www.snpedia.com/index.php?title=Rs16947078 reference = Chr18 snp rs16949646 44392073..44392073 "breast cancer strong linkage disequilibrium for rs16949646 rs2302254 and rs3760468" http://www.snpedia.com/index.php?title=Rs16949646 reference = Chr17 both rs16949649 46585307..46585307 "breast cancer 1,134 breast cancer patients recruited as part of the Shanghai Breast Cancer Study who..." http://www.snpedia.com/index.php?title=Rs16949649 reference = Chr11 illumina rs1695 67109265..67109265 "This snp, in the GSTP1 gene influences asthma risk mentioned in this [http://news.bbc.co.uk/2/hi/uk_..." http://www.snpedia.com/index.php?title=Rs1695 reference = Chr13 illumina rs169547 31827387..31827387 "" http://www.snpedia.com/index.php?title=Rs169547 reference = Chr15 both rs16964201 49302643..49302643 "The research paper suggests that the 3 snps rs17703883, rs12594287 and rs16964201 affect bone miner..." http://www.snpedia.com/index.php?title=Rs16964201 reference = Chr15 snp rs16964465 49759639..49759639 "rs16964465 rs16964476 may influence the risk of obesity through possible regulation of hypothalamic ..." http://www.snpedia.com/index.php?title=Rs16964465 reference = Chr15 snp rs16964476 49761516..49761516 "rs16964465 rs16964476 may influence the risk of obesity through possible regulation of hypothalamic ..." http://www.snpedia.com/index.php?title=Rs16964476 reference = Chr15 illumina rs16969968 76669980..76669980 "Associated with smoking phenotype (p=0.007) based on association study of 2,000+ individuals, and fu..." http://www.snpedia.com/index.php?title=Rs16969968 reference = Chr5 both rs1697144 66515760..66515760 "" http://www.snpedia.com/index.php?title=Rs1697144 reference = ChrNone illumina rs16980360 14318720..14318720 "" http://www.snpedia.com/index.php?title=Rs16980360 reference = ChrNone affy rs16980363 14712374..14712374 "" http://www.snpedia.com/index.php?title=Rs16980363 reference = ChrNone snp rs16980370 14987946..14987946 "" http://www.snpedia.com/index.php?title=Rs16980370 reference = ChrY both rs16980391 17087870..17087870 "" http://www.snpedia.com/index.php?title=Rs16980391 reference = ChrY illumina rs16980394 17745841..17745841 "" http://www.snpedia.com/index.php?title=Rs16980394 reference = ChrY both rs16980396 17859009..17859009 "" http://www.snpedia.com/index.php?title=Rs16980396 reference = ChrY affy rs16980406 20105446..20105446 "" http://www.snpedia.com/index.php?title=Rs16980406 reference = ChrY both rs16980426 20673609..20673609 "" http://www.snpedia.com/index.php?title=Rs16980426 reference = ChrNone illumina rs16980473 12669846..12669846 "" http://www.snpedia.com/index.php?title=Rs16980473 reference = ChrNone snp rs16980478 12709284..12709284 "" http://www.snpedia.com/index.php?title=Rs16980478 reference = ChrNone snp rs16980495 16687485..16687485 "" http://www.snpedia.com/index.php?title=Rs16980495 reference = ChrNone illumina rs16980499 15765412..15765412 "" http://www.snpedia.com/index.php?title=Rs16980499 reference = ChrNone illumina rs16980502 15804352..15804352 "" http://www.snpedia.com/index.php?title=Rs16980502 reference = ChrY both rs16980548 21327965..21327965 "" http://www.snpedia.com/index.php?title=Rs16980548 reference = ChrNone both rs16980558 14088609..14088609 "" http://www.snpedia.com/index.php?title=Rs16980558 reference = ChrY snp rs16980574 20077971..20077971 "" http://www.snpedia.com/index.php?title=Rs16980574 reference = ChrY snp rs16980577 19542808..19542808 "" http://www.snpedia.com/index.php?title=Rs16980577 reference = ChrNone affy rs16980586 14760751..14760751 "" http://www.snpedia.com/index.php?title=Rs16980586 reference = ChrNone both rs16980588 14763088..14763088 "" http://www.snpedia.com/index.php?title=Rs16980588 reference = ChrNone affy rs16980589 14883820..14883820 "" http://www.snpedia.com/index.php?title=Rs16980589 reference = ChrY affy rs16980598 17880310..17880310 "" http://www.snpedia.com/index.php?title=Rs16980598 reference = ChrNone affy rs16980601 13924509..13924509 "" http://www.snpedia.com/index.php?title=Rs16980601 reference = ChrY snp rs16980610 22043750..22043750 "" http://www.snpedia.com/index.php?title=Rs16980610 reference = ChrNone snp rs16980621 12570308..12570308 "" http://www.snpedia.com/index.php?title=Rs16980621 reference = Chr21 snp rs1698064 32077478..32077478 "" http://www.snpedia.com/index.php?title=Rs1698064 reference = ChrY snp rs16980711 10476740..10476740 "" http://www.snpedia.com/index.php?title=Rs16980711 reference = ChrY illumina rs16980749 7392132..7392132 "" http://www.snpedia.com/index.php?title=Rs16980749 reference = ChrY both rs16981290 7628568..7628568 "" http://www.snpedia.com/index.php?title=Rs16981290 reference = ChrY both rs16981293 8856078..8856078 "" http://www.snpedia.com/index.php?title=Rs16981293 reference = ChrY illumina rs16981297 8835178..8835178 "" http://www.snpedia.com/index.php?title=Rs16981297 reference = ChrY both rs16981311 7025215..7025215 "" http://www.snpedia.com/index.php?title=Rs16981311 reference = ChrY snp rs16981340 8662415..8662415 "" http://www.snpedia.com/index.php?title=Rs16981340 reference = Chr20 illumina rs16990018 4628378..4628378 "[omim:SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES]" http://www.snpedia.com/index.php?title=Rs16990018 reference = Chr11 affy rs1699103 120957136..120957136 "rs1699103 is among several SNPs in the SORL1 gene that show some association with increased (or decr..." http://www.snpedia.com/index.php?title=Rs1699103 reference = Chr22 snp rs17001266 38246576..38246576 "This SNP is on its own, as well as part of a specific haplotype, associated with an overall higher r..." http://www.snpedia.com/index.php?title=Rs17001266 reference = Chr12 affy rs17005598 78358864..78358864 "" http://www.snpedia.com/index.php?title=Rs17005598 reference = Chr2 snp rs17027230 102445762..102445762 "This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients." http://www.snpedia.com/index.php?title=Rs17027230 reference = Chr4 illumina rs17029215 100740828..100740828 "" http://www.snpedia.com/index.php?title=Rs17029215 reference = Chr3 snp rs17036314 12351745..12351745 "rs17036314 is a SNP in the peroxisome proliferator-activated receptor gamma PPARG gene. In a 4 year ..." http://www.snpedia.com/index.php?title=Rs17036314 reference = Chr2 affy rs17041183 51083159..51083159 "rs17041183 is in linkage disequilibrium with a polymorphism that increases susceptibility to Substan..." http://www.snpedia.com/index.php?title=Rs17041183 reference = Chr4 affy rs17044137 113014746..113014746 "rs17044137 increases susceptibility to Type II Diabetes 1.13 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs17044137 reference = Chr5 affy rs17070145 167778369..167778369 "In a Swiss cohort: 'Carriers of KIBRA rs17070145 T allele had 24% better free recall performance 5 m..." http://www.snpedia.com/index.php?title=Rs17070145 reference = Chr6 illumina rs17073260 112489016..112489016 "[omim:ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD]" http://www.snpedia.com/index.php?title=Rs17073260 reference = Chr6 both rs1709183 152235689..152235689 "rs1709183 associated with EDV endothelium-dependent vasodilation in resistance, but not conduit arte..." http://www.snpedia.com/index.php?title=Rs1709183 reference = Chr10 illumina rs17098707 121076087..121076087 "This polymorphism is present in the GRK5 gene found on chromosome 10 and leads to a nonsynonymous ch..." http://www.snpedia.com/index.php?title=Rs17098707 reference = Chr5 illumina rs17107315 147187871..147187871 "[omim:PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs17107315 reference = Chr12 illumina rs17110563 70652573..70652573 "rs17110563, also known as Pro206Ser, is a SNP in the TPH2 gene. The minor allele of this SNP yielded..." http://www.snpedia.com/index.php?title=Rs17110563 reference = Chr10 affy rs17116350 105783740..105783740 "" http://www.snpedia.com/index.php?title=Rs17116350 reference = Chr12 snp rs17120527 63302567..63302567 "" http://www.snpedia.com/index.php?title=Rs17120527 reference = Chr7 illumina rs17137124 113998050..113998050 "variations in rs17137124 and rs10227893 may impair speech" http://www.snpedia.com/index.php?title=Rs17137124 reference = Chr7 both rs17145738 72620810..72620810 "rs17145738 influences severe hypertriglyceridemia. 132 patients of European ancestry with severe HTG..." http://www.snpedia.com/index.php?title=Rs17145738 reference = Chr10 illumina rs17158558 42940341..42940341 "A complex pattern of mutations involving rs17158558(T) and other mutations simultaneously occurring ..." http://www.snpedia.com/index.php?title=Rs17158558 reference = Chr5 affy rs17166496 132656783..132656783 "rs17166496 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs17166496 reference = ChrY snp rs17174528 9168252..9168252 "" http://www.snpedia.com/index.php?title=Rs17174528 reference = Chr8 snp rs1721082 16894503..16894503 "Associated with Parkinson's disease based on a conditional logistic regression analysis." http://www.snpedia.com/index.php?title=Rs1721082 reference = Chr8 affy rs1721100 16894869..16894869 "Parkinson's disease The risk alleles for each SNP identified from conditional logistic regression, r..." http://www.snpedia.com/index.php?title=Rs1721100 reference = Chr6 snp rs17211036 32605895..32605895 "" http://www.snpedia.com/index.php?title=Rs17211036 reference = Chr11 snp rs17215437 73846009..73846009 "[omim:HYPOKALEMIC PERIODIC PARALYSIS]" http://www.snpedia.com/index.php?title=Rs17215437 reference = Chr13 snp rs17216473 30201965..30201965 "rs17216473, also known as SG13S377, is an ALOX5AP gene SNP that has been defined as part of a haplot..." http://www.snpedia.com/index.php?title=Rs17216473 reference = Chr16 affy rs17221417 49297083..49297083 "rs17221417 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs17221417 reference = ChrNone both rs17221964 14027245..14027245 "" http://www.snpedia.com/index.php?title=Rs17221964 reference = ChrNone affy rs17222244 15208728..15208728 "" http://www.snpedia.com/index.php?title=Rs17222244 reference = ChrNone illumina rs17222279 15348893..15348893 "" http://www.snpedia.com/index.php?title=Rs17222279 reference = ChrNone illumina rs17222419 16017731..16017731 "" http://www.snpedia.com/index.php?title=Rs17222419 reference = Chr13 snp rs17222814 30197553..30197553 "rs17222814, also known as SG13S25, is an ALOX5AP gene SNP that has been defined as part of a haploty..." http://www.snpedia.com/index.php?title=Rs17222814 reference = Chr13 snp rs17222842 30238117..30238117 "rs17222842, also known as SG13S35, is an ALOX5AP gene SNP that has been defined as part of a haploty..." http://www.snpedia.com/index.php?title=Rs17222842 reference = Chr15 affy rs17228212 65245693..65245693 "rs17228212 is a SNP found to be associated with heart disease by the German MI (Myocardial infarctio..." http://www.snpedia.com/index.php?title=Rs17228212 reference = Chr5 both rs17234657 40437266..40437266 "rs17234657 has been reported in a large study to be associated with Crohn's disease. The risk allele..." http://www.snpedia.com/index.php?title=Rs17234657 reference = Chr5 snp rs17238540 74691254..74691254 "rs17238540, also known as SNP 29, is located in the HMG-CoA reductase HMGCR gene. The protein encode..." http://www.snpedia.com/index.php?title=Rs17238540 reference = Chr5 snp rs17244841 74678611..74678611 "rs17244841, also known as SNP 12, is located in the HMG-CoA reductase HMGCR gene. The protein encode..." http://www.snpedia.com/index.php?title=Rs17244841 reference = Chr15 illumina rs1724577 50476923..50476923 "" http://www.snpedia.com/index.php?title=Rs1724577 reference = ChrY snp rs17249974 17776738..17776738 "" http://www.snpedia.com/index.php?title=Rs17249974 reference = ChrY both rs17250121 19296941..19296941 "" http://www.snpedia.com/index.php?title=Rs17250121 reference = ChrY snp rs17250163 19685158..19685158 "" http://www.snpedia.com/index.php?title=Rs17250163 reference = ChrY affy rs17250887 8618969..8618969 "" http://www.snpedia.com/index.php?title=Rs17250887 reference = ChrY snp rs17250992 8905380..8905380 "" http://www.snpedia.com/index.php?title=Rs17250992 reference = Chr4 affy rs17266594 102969945..102969945 "rs17266594 rs10516487 rs3733197 gene associated with systemic lupus erythematosus." http://www.snpedia.com/index.php?title=Rs17266594 reference = Chr7 illumina rs1726866 141319174..141319174 "rs1726866 is one of three SNPs that form the main haplotypes behind the ability to perceive as bitte..." http://www.snpedia.com/index.php?title=Rs1726866 reference = ChrNone both rs17269816 15563165..15563165 "" http://www.snpedia.com/index.php?title=Rs17269816 reference = ChrY both rs17269928 17156436..17156436 "" http://www.snpedia.com/index.php?title=Rs17269928 reference = ChrY affy rs17276358 17688857..17688857 "" http://www.snpedia.com/index.php?title=Rs17276358 reference = Chr1 illumina rs17292650 43576394..43576394 "[omim:THROMBOCYTOSIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs17292650 reference = ChrNone affy rs17306657 12502338..12502338 "" http://www.snpedia.com/index.php?title=Rs17306657 reference = ChrNone affy rs17306671 12541334..12541334 "" http://www.snpedia.com/index.php?title=Rs17306671 reference = ChrNone snp rs17306699 12654593..12654593 "" http://www.snpedia.com/index.php?title=Rs17306699 reference = ChrNone both rs17307070 14099736..14099736 "" http://www.snpedia.com/index.php?title=Rs17307070 reference = ChrNone snp rs17307294 15148198..15148198 "" http://www.snpedia.com/index.php?title=Rs17307294 reference = ChrNone illumina rs17307398 15795387..15795387 "" http://www.snpedia.com/index.php?title=Rs17307398 reference = ChrNone illumina rs17307656 16538055..16538055 "" http://www.snpedia.com/index.php?title=Rs17307656 reference = Chr16 illumina rs1731017 8747455..8747455 "" http://www.snpedia.com/index.php?title=Rs1731017 reference = ChrY affy rs17315680 17256887..17256887 "" http://www.snpedia.com/index.php?title=Rs17315680 reference = ChrY affy rs17315723 17397594..17397594 "" http://www.snpedia.com/index.php?title=Rs17315723 reference = ChrY illumina rs17315758 17473657..17473657 "" http://www.snpedia.com/index.php?title=Rs17315758 reference = ChrY both rs17315772 17547696..17547696 "" http://www.snpedia.com/index.php?title=Rs17315772 reference = ChrY both rs17315821 17676255..17676255 "" http://www.snpedia.com/index.php?title=Rs17315821 reference = ChrY affy rs17315835 17688729..17688729 "" http://www.snpedia.com/index.php?title=Rs17315835 reference = ChrNone both rs17316007 12511232..12511232 "" http://www.snpedia.com/index.php?title=Rs17316007 reference = ChrY illumina rs17316592 17069399..17069399 "" http://www.snpedia.com/index.php?title=Rs17316592 reference = ChrY snp rs17316597 7608915..7608915 "" http://www.snpedia.com/index.php?title=Rs17316597 reference = ChrY both rs17316729 8413707..8413707 "" http://www.snpedia.com/index.php?title=Rs17316729 reference = ChrY both rs17316910 22885057..22885057 "" http://www.snpedia.com/index.php?title=Rs17316910 reference = Chr8 affy rs17321515 126555591..126555591 "rs17321515 influences severe hypertriglyceridemia. 132 patients of European ancestry with severe HTG..." http://www.snpedia.com/index.php?title=Rs17321515 reference = Chr7 snp rs17329669 36818454..36818454 "rs17329669 increases susceptibility to Parkinson's disease 1.71 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs17329669 reference = Chr8 both rs17337252 53749259..53749259 "" http://www.snpedia.com/index.php?title=Rs17337252 reference = ChrX both rs1734787 152978640..152978640 "rs1734787 is one of several SNPs in the methyl CpG binding protein 2 (MECP2) that have been associat..." http://www.snpedia.com/index.php?title=Rs1734787 reference = ChrX affy rs1734791 152984114..152984114 "rs1734791 is one of several SNPs in the methyl CpG binding protein 2 (MECP2) that have been associat..." http://www.snpedia.com/index.php?title=Rs1734791 reference = ChrX both rs1734792 152994254..152994254 "rs1734792 is one of several SNPs in the methyl CpG binding protein 2 (MECP2) that have been associat..." http://www.snpedia.com/index.php?title=Rs1734792 reference = Chr5 both rs173686 82847256..82847256 "The presence of an rs173686(C) allele has been linked to increased risk of a certain type of stroke,..." http://www.snpedia.com/index.php?title=Rs173686 reference = Chr1 affy rs17374983 162113964..162113964 "" http://www.snpedia.com/index.php?title=Rs17374983 reference = Chr4 both rs17388568 123548812..123548812 "rs17388568 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs17388568 reference = Chr8 affy rs17411031 19896590..19896590 "rs17411031 increases susceptibility to Coronary artery disease 1.23 times for carriers of the G alle..." http://www.snpedia.com/index.php?title=Rs17411031 reference = ChrX affy rs17435 152965174..152965174 "rs17435 is one of several SNPs in the methyl CpG binding protein 2 (MECP2) that have been associated..." http://www.snpedia.com/index.php?title=Rs17435 reference = Chr11 snp rs174575 61358579..61358579 "A SNP in the FADS2 gene, rs174575, has been linked to increased intelligence (as measured on IQ test..." http://www.snpedia.com/index.php?title=Rs174575 reference = Chr1 affy rs17465637 220890152..220890152 "rs17465637 is a SNP found to be associated with heart disease by the German MI (Myocardial infarctio..." http://www.snpedia.com/index.php?title=Rs17465637 reference = Chr1 snp rs17472401 5862830..5862830 "" http://www.snpedia.com/index.php?title=Rs17472401 reference = Chr1 snp rs1748031 17535494..17535494 "rs1748031 increases susceptibility to Rheumatoid Arthritis 1.92 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs1748031 reference = Chr1 illumina rs1748033 17535249..17535249 "rs1748033 increases susceptibility to Rheumatoid Arthritis 1.09 times for heterozygotes (AG) and 1.1..." http://www.snpedia.com/index.php?title=Rs1748033 reference = Chr1 affy rs1748035 17534583..17534583 "rs1748035 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumato..." http://www.snpedia.com/index.php?title=Rs1748035 reference = Chr5 illumina rs17482078 96144622..96144622 "rs17482078 is one of several SNPs in the ARTS1 gene that has been shown in a large (over 1,000 Cauca..." http://www.snpedia.com/index.php?title=Rs17482078 reference = Chr8 affy rs17482753 19876926..19876926 "rs17482753 increases susceptibility to Elevated HDL-Cholesterol for carriers of the T allele rs1748..." http://www.snpedia.com/index.php?title=Rs17482753 reference = Chr2 both rs17483466 111513929..111513929 "[http://spittoon.23andme.com/2008/08/31/snpwatch-researchers-find-first-snps-linked-to-common-type-o..." http://www.snpedia.com/index.php?title=Rs17483466 reference = Chr15 both rs17483721 76520786..76520786 "rs17483721 increases susceptibility to Lung cancer 1.27 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs17483721 reference = Chr15 affy rs17483929 76529431..76529431 "rs17483929 increases susceptibility to Lung cancer 1.29 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs17483929 reference = Chr15 affy rs17487223 76711042..76711042 "rs17487223 increases susceptibility to Lung cancer 1.28 times for carriers of the T allele [http://..." http://www.snpedia.com/index.php?title=Rs17487223 reference = Chr8 affy rs17489268 19896325..19896325 "rs17489268 increases susceptibility to Coronary artery disease 1.25 times for carriers of the A alle..." http://www.snpedia.com/index.php?title=Rs17489268 reference = Chr14 illumina rs175081 74583636..74583636 "" http://www.snpedia.com/index.php?title=Rs175081 reference = Chr22 illumina rs175174 18507554..18507554 "This snp in the gene ZDHHC8 does not appear to have any link to schizophrenia despite being quite po..." http://www.snpedia.com/index.php?title=Rs175174 reference = Chr7 affy rs17562004 7868894..7868894 "rs17562004 is in linkage disequilibrium with a polymorphism that increases susceptibility to Prostat..." http://www.snpedia.com/index.php?title=Rs17562004 reference = Chr14 both rs17563 53487272..53487272 "rs17563(G) allele, coding for the amino acid alanine, confers susceptibility to otosclerosis (combin..." http://www.snpedia.com/index.php?title=Rs17563 reference = Chr1 both rs17567 51599509..51599509 "" http://www.snpedia.com/index.php?title=Rs17567 reference = Chr11 illumina rs17571 1739170..1739170 "[http://7thspace.com/headlines/279477/cathepsin_d_snp_associated_with_increased_risk_of_variant_creu..." http://www.snpedia.com/index.php?title=Rs17571 reference = Chr20 illumina rs17576 44073632..44073632 "rs17576, also known as Gln279Arg or Q279R, is a SNP in exon 6 of the matrix metalloproteinase-9 MMP9..." http://www.snpedia.com/index.php?title=Rs17576 reference = Chr14 snp rs17580 93917015..93917015 "[omim:PI S]" http://www.snpedia.com/index.php?title=Rs17580 reference = Chr1 affy rs17602729 115037580..115037580 "rs17602729, a SNP located in the AMPD1 gene and also known as 'C34T', has at times been called the '..." http://www.snpedia.com/index.php?title=Rs17602729 reference = Chr19 illumina rs17608 44917486..44917486 "" http://www.snpedia.com/index.php?title=Rs17608 reference = Chr18 snp rs17647532 31488070..31488070 "rs17647532 is a SNP in the GALNT1 gene that has a variant rarely seen in ovarian cancer, which may i..." http://www.snpedia.com/index.php?title=Rs17647532 reference = Chr17 both rs17651507 41414847..41414847 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs17651507 reference = Chr13 snp rs17655 102326003..102326003 "" http://www.snpedia.com/index.php?title=Rs17655 reference = Chr1 affy rs17672135 238512219..238512219 "rs17672135 has been reported in a large study to be associated with heart disease, in particular, co..." http://www.snpedia.com/index.php?title=Rs17672135 reference = Chr9 illumina rs1769259 96408970..96408970 "" http://www.snpedia.com/index.php?title=Rs1769259 reference = Chr12 both rs17696736 110971201..110971201 "rs17696736 has been reported in a large study to be associated with type-1 diabetes. The risk allele..." http://www.snpedia.com/index.php?title=Rs17696736 reference = Chr15 both rs17703883 49317389..49317389 "The research paper suggests that the 3 snps rs17703883, rs12594287 and rs16964201 affect bone miner..." http://www.snpedia.com/index.php?title=Rs17703883 reference = Chr4 affy rs17781557 3118451..3118451 "" http://www.snpedia.com/index.php?title=Rs17781557 reference = Chr18 affy rs17782313 56002077..56002077 "A study of 60,000 adults indicates that rs17782313(C) alleles are associated with higher body mass i..." http://www.snpedia.com/index.php?title=Rs17782313 reference = Chr16 illumina rs17817449 52370868..52370868 "Within the FTO gene, many SNPs appear to be co-inherited. The SNP showing the strongest association ..." http://www.snpedia.com/index.php?title=Rs17817449 reference = Chr16 both rs17822931 46815699..46815699 "This SNP determines wet vs dry earwax as well as sweat production it is commonly (T;T) for asians an..." http://www.snpedia.com/index.php?title=Rs17822931 reference = ChrY both rs17842387 8484089..8484089 "" http://www.snpedia.com/index.php?title=Rs17842387 reference = ChrY both rs17842518 21853359..21853359 "" http://www.snpedia.com/index.php?title=Rs17842518 reference = Chr21 snp rs17846179 34743691..34743691 "" http://www.snpedia.com/index.php?title=Rs17846179 reference = Chr11 snp rs17848368 73394991..73394991 "[omim:OBESITY, SEVERE, AND TYPE II DIABETES]" http://www.snpedia.com/index.php?title=Rs17848368 reference = Chr11 affy rs1784931 120988148..120988148 "rs1784931 is among several SNPs in the SORL1 gene that show some association with increased (or decr..." http://www.snpedia.com/index.php?title=Rs1784931 reference = Chr13 snp rs17849654 40280711..40280711 "" http://www.snpedia.com/index.php?title=Rs17849654 reference = Chr19 snp rs17855739 5782840..5782840 "[omim:FUCOSYLTRANSFERASE-6 DEFICIENCY, PLASMA, INDONESIAN TYPE]" http://www.snpedia.com/index.php?title=Rs17855739 reference = Chr8 snp rs17855765 145612136..145612136 "" http://www.snpedia.com/index.php?title=Rs17855765 reference = Chr1 snp rs17856039 63654140..63654140 "" http://www.snpedia.com/index.php?title=Rs17856039 reference = Chr17 snp rs17856697 7289349..7289349 "" http://www.snpedia.com/index.php?title=Rs17856697 reference = Chr2 snp rs17860403 201781082..201781082 "[omim:AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA]" http://www.snpedia.com/index.php?title=Rs17860403 reference = Chr2 snp rs17860424 201849876..201849876 "[omim:CASPASE 8 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs17860424 reference = Chr5 snp rs17876030 176764432..176764432 "" http://www.snpedia.com/index.php?title=Rs17876030 reference = Chr22 illumina rs17879961 27451087..27451087 "This SNP, a variant in the CHEK2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs17879961 reference = ChrNone snp rs17883192 1431542..1431542 "rs17883192, part of a haplotype block spanning introns 4, 5 and 6 of the IL3RA gene, has been report..." http://www.snpedia.com/index.php?title=Rs17883192 reference = Chr17 snp rs17887200 7511796..7511796 "rs17887200 and rs12951053 associated with ER negative breast cancer tumors (1.48 (1.11-1.93) p-trend..." http://www.snpedia.com/index.php?title=Rs17887200 reference = Chr18 illumina rs1788799 19378943..19378943 "" http://www.snpedia.com/index.php?title=Rs1788799 reference = Chr11 both rs1792113 120970156..120970156 "rs1792113 is among several SNPs in the SORL1 gene that show some association with increased (or decr..." http://www.snpedia.com/index.php?title=Rs1792113 reference = Chr11 affy rs1793004 20655505..20655505 "rs1793004 is a SNP in the NELL1 gene that was found in a genome-wide association study to be associa..." http://www.snpedia.com/index.php?title=Rs1793004 reference = Chr9 illumina rs1796993 74505258..74505258 "" http://www.snpedia.com/index.php?title=Rs1796993 reference = Chr6 snp rs1799724 31650461..31650461 "rs1799724, a SNP in the tumor necrosis factor TNF gene, was found in a study of ~500 Caucasians to b..." http://www.snpedia.com/index.php?title=Rs1799724 reference = Chr11 snp rs1799750 102175706..102175706 "rs1799750 is a SNP at position -1,607 of the promoter of the MMP1 gene, consisting of an insertion p..." http://www.snpedia.com/index.php?title=Rs1799750 reference = Chr17 snp rs1799752 58919622..58919622 "rs1799752 is one of four SNPs representing perhaps the best studied ACE SNP. It is actually not a si..." http://www.snpedia.com/index.php?title=Rs1799752 reference = Chr7 snp rs1799762 100556428..100556428 "This SNP is equivalent to, and therefore please go to, rs1799889 for related information." http://www.snpedia.com/index.php?title=Rs1799762 reference = Chr7 snp rs1799768 100556426..100556426 "This SNP is equivalent to, and therefore please go to, rs1799889 for related information." http://www.snpedia.com/index.php?title=Rs1799768 reference = Chr19 snp rs1799782 48749414..48749414 "rs1799782, a SNP also known as Arg194Trp located in the DNA-repair gene XRCC1, is associated with a ..." http://www.snpedia.com/index.php?title=Rs1799782 reference = Chr19 snp rs1799793 50559099..50559099 "" http://www.snpedia.com/index.php?title=Rs1799793 reference = Chr3 both rs1799807 167031223..167031223 "[omim:APNEA, POSTANESTHETIC, DUE TO BCHE, ATYPICAL-1]" http://www.snpedia.com/index.php?title=Rs1799807 reference = Chr1 both rs1799821 53449036..53449036 "" http://www.snpedia.com/index.php?title=Rs1799821 reference = ChrX both rs1799836 43512943..43512943 "Parkinson's disease The risk alleles for each SNP identified from conditional logistic regression, r..." http://www.snpedia.com/index.php?title=Rs1799836 reference = Chr10 snp rs1799853 96692037..96692037 "rs1799853 is a SNP in the CYP2C9 gene. The rs1799853(T) allele encodes a variant amino acid, cystein..." http://www.snpedia.com/index.php?title=Rs1799853 reference = Chr3 snp rs1799864 46374212..46374212 "Compared with individuals without CCR5-Delta32 (a variation in another gene) or rs1799864(A), indivi..." http://www.snpedia.com/index.php?title=Rs1799864 reference = Chr7 affy rs1799884 44195593..44195593 "rs1799884, known also as the -30 SNP of the GCK gene, has been associated with type-2 diabetes. This..." http://www.snpedia.com/index.php?title=Rs1799884 reference = Chr7 snp rs1799889 100556430..100556430 "rs1799889 is an insertion/deletion polymorphism in the promoter region of the SERPINE1 gene, which i..." http://www.snpedia.com/index.php?title=Rs1799889 reference = Chr3 illumina rs1799899 134958502..134958502 "it was concluded that PAI-1 promoter polymorphism 4G -> 5G (rs1799899) is not associated with the ag..." http://www.snpedia.com/index.php?title=Rs1799899 reference = Chr11 snp rs1799913 18003831..18003831 "Only for Hispanics, individuals who have a genoset composed of rs1799913(C;C) and rs7963720(T;T) are..." http://www.snpedia.com/index.php?title=Rs1799913 reference = Chr8 both rs1799929 18302274..18302274 "rs1799929 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1799929 reference = Chr8 both rs1799930 18302383..18302383 "rs1799930 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1799930 reference = Chr8 illumina rs1799931 18302650..18302650 "rs1799931 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1799931 reference = Chr10 illumina rs1799939 42930125..42930125 "" http://www.snpedia.com/index.php?title=Rs1799939 reference = Chr13 both rs1799944 31809463..31809463 "One form of this SNP, known as N991D for the nonsynonymous change it produces in the BRCA2 protein, ..." http://www.snpedia.com/index.php?title=Rs1799944 reference = Chr8 illumina rs1799946 6722841..6722841 "found no association with Crohn's disease for rs1799946, but did find associations for two other DEF..." http://www.snpedia.com/index.php?title=Rs1799946 reference = Chr17 illumina rs1799950 38500007..38500007 "This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs1799950 reference = Chr13 illumina rs1799954 31812592..31812592 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs1799954 reference = Chr11 snp rs1799963 46717631..46717631 "rs1799963 is a SNP far more commonly known as the G20210A mutation of the prothrombin F2 gene. Due t..." http://www.snpedia.com/index.php?title=Rs1799963 reference = Chr6 affy rs1799964 31650287..31650287 "Associated with at least one 'mortality outcome' in a study of ~10,000 individuals. Separately, a me..." http://www.snpedia.com/index.php?title=Rs1799964 reference = Chr17 illumina rs1799966 38476620..38476620 "This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs1799966 reference = Chr19 illumina rs1799969 10255792..10255792 "rs1799969, also known as G241R or +241G/A, is a SNP in the ICAM1 gene. The more common (G) allele en..." http://www.snpedia.com/index.php?title=Rs1799969 reference = Chr6 illumina rs1799971 154402490..154402490 "The rs1799971(G) allele in exon 1 of the mu opiod receptor gene causes the normal amino acid at resi..." http://www.snpedia.com/index.php?title=Rs1799971 reference = Chr7 snp rs1799983 150327044..150327044 "rs1799983, a SNP also known as Glu298Asp or E298D and located in the NOS3 gene, was associated with ..." http://www.snpedia.com/index.php?title=Rs1799983 reference = Chr20 illumina rs1799990 4628251..4628251 "[omim:PRION DISEASE, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1799990 reference = Chr7 both rs1799999 113305670..113305670 "[omim:INSULIN RESISTANCE, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1799999 reference = Chr11 both rs1800056 107643213..107643213 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs1800056 reference = Chr11 illumina rs1800057 107648666..107648666 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs1800057 reference = Chr11 illumina rs1800058 107665560..107665560 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs1800058 reference = Chr16 illumina rs1800067 13936534..13936534 "" http://www.snpedia.com/index.php?title=Rs1800067 reference = Chr7 snp rs1800098 116824405..116824405 "[omim:VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF]" http://www.snpedia.com/index.php?title=Rs1800098 reference = Chr11 illumina rs1800169 58148077..58148077 "rs1800169 is a SNP in the ciliary neurotrophic factor CNTF gene. In a study of 417 patients with sch..." http://www.snpedia.com/index.php?title=Rs1800169 reference = Chr17 illumina rs1800215 45620494..45620494 "" http://www.snpedia.com/index.php?title=Rs1800215 reference = ChrX illumina rs1800278 31406347..31406347 "[omim:DUCHENNE MUSCULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs1800278 reference = ChrX illumina rs1800280 31406271..31406271 "" http://www.snpedia.com/index.php?title=Rs1800280 reference = Chr17 illumina rs1800309 75701636..75701636 "[omim:ACID ALPHA-GLUCOSIDASE, ALLELE 4]" http://www.snpedia.com/index.php?title=Rs1800309 reference = ChrX both rs1800321 38111547..38111547 "[omim:ORNITHINE TRANSCARBAMYLASE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800321 reference = Chr12 illumina rs1800378 6042463..6042463 "" http://www.snpedia.com/index.php?title=Rs1800378 reference = Chr15 snp rs1800401 25933648..25933648 "rs1800401 is located in exon 7 of the OCA2 gene at amino acid position 305. The (T) allele encodes t..." http://www.snpedia.com/index.php?title=Rs1800401 reference = Chr15 illumina rs1800407 25903913..25903913 "rs1800407 is located in exon 13 of the OCA2 gene at amino acid position 419, and it is therefore als..." http://www.snpedia.com/index.php?title=Rs1800407 reference = Chr15 illumina rs1800431 70425946..70425946 "" http://www.snpedia.com/index.php?title=Rs1800431 reference = Chr9 snp rs1800435 115193712..115193712 "[omim:AMINOLEVULINATE DEHYDRATASE, ALAD*1/ALAD*2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800435 reference = Chr19 snp rs1800437 50873232..50873232 "SNP rs1800437, located in the coding region of the GIPR gene and known as Glu354Gln, shows a margina..." http://www.snpedia.com/index.php?title=Rs1800437 reference = Chr11 illumina rs1800443 629830..629830 "[omim:DOPAMINE RECEPTOR D4 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800443 reference = Chr19 snp rs1800447 54211717..54211717 "[omim:LUTEINIZING HORMONE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800447 reference = Chr5 illumina rs1800449 121441107..121441107 "[omim:LYSYL OXIDASE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800449 reference = Chr10 illumina rs1800450 54201241..54201241 "pulmonary morbidity in preterm infants. related to non-Hodgkin's lymphoma [omim:MANNOSE-BINDING PRO..." http://www.snpedia.com/index.php?title=Rs1800450 reference = Chr6 both rs1800454 32908390..32908390 "[omim:PEPTIDE TRANSPORTER PSF2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800454 reference = Chr18 illumina rs1800458 27426863..27426863 "[omim:TRANSTHYRETIN SER-6 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1800458 reference = Chr6 illumina rs1800460 18247207..18247207 "rs1800460 is a SNP in the TPMT gene, potentially encoding a variant incapable of detoxifying byprodu..." http://www.snpedia.com/index.php?title=Rs1800460 reference = Chr6 snp rs1800462 18251934..18251934 "rs1800462 is a rare SNP in the TPMT gene, potentially encoding a variant incapable of detoxifying by..." http://www.snpedia.com/index.php?title=Rs1800462 reference = Chr19 illumina rs1800469 46552136..46552136 "rs1800469, a SNP in the promoter region of the transforming growth factor beta1 TGFB1 gene has been ..." http://www.snpedia.com/index.php?title=Rs1800469 reference = Chr19 snp rs1800471 46550716..46550716 "rs1800471 encodes a change at codon 25 of the TGFB1 gene. It is reported to predispose several organ..." http://www.snpedia.com/index.php?title=Rs1800471 reference = Chr11 snp rs1800496 112788698..112788698 "[http://originsgenomeresources.net/musings/?p=36 origins] associated with an independent aspect of d..." http://www.snpedia.com/index.php?title=Rs1800496 reference = Chr11 illumina rs1800497 112776038..112776038 "rs1800497, a SNP also known as the TaqIA (or Taq1A) polymorphism of the dopamine D2 receptor DRD2 ge..." http://www.snpedia.com/index.php?title=Rs1800497 reference = Chr11 affy rs1800532 18004392..18004392 "rs211105, rs1800532 and rs7933505 related to schizophrenia" http://www.snpedia.com/index.php?title=Rs1800532 reference = Chr17 illumina rs1800547 41407682..41407682 "significantly associated with parkinson's disease" http://www.snpedia.com/index.php?title=Rs1800547 reference = Chr12 illumina rs1800556 119660061..119660061 "" http://www.snpedia.com/index.php?title=Rs1800556 reference = Chr6 both rs1800562 26201120..26201120 "rs1800562 represents a SNP that accounts for ~85% of all cases of hemochromatosis, a disorder who's ..." http://www.snpedia.com/index.php?title=Rs1800562 reference = Chr16 both rs1800566 68302646..68302646 "[http://spittoon.23andme.com/2008/06/01/snpwatch-gene-variant-may-be-a-strong-predictive-factor-in-b..." http://www.snpedia.com/index.php?title=Rs1800566 reference = Chr2 both rs1800587 113259431..113259431 "rs1800587 increases susceptibility to Intervertebral disc disease 1.31 times for heterozygotes (CT) ..." http://www.snpedia.com/index.php?title=Rs1800587 reference = Chr15 snp rs1800588 56510967..56510967 "rs1800588, also known as the -514C/T polymorphism of the LIPC gene, may influence the levels of the ..." http://www.snpedia.com/index.php?title=Rs1800588 reference = Chr6 snp rs1800610 31651806..31651806 "rs1800610 increases susceptibility to Type II Diabetes 1.42 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs1800610 reference = Chr6 illumina rs1800629 31651010..31651010 "rs1800629 is also known as the TNF -308 SNP, and occasionally the rs1800629(A) allele is referred to..." http://www.snpedia.com/index.php?title=Rs1800629 reference = Chr6 illumina rs1800630 31650455..31650455 "rs1800630 is a SNP upstream of the tumor necrosis alpha (TNF) gene; this SNP is also typically calle..." http://www.snpedia.com/index.php?title=Rs1800630 reference = Chr17 illumina rs1800709 38498553..38498553 "[omim:BREAST CANCER]" http://www.snpedia.com/index.php?title=Rs1800709 reference = Chr3 both rs1800734 37009950..37009950 "colorectal cancer (-93G>A, rs1800734) 1,518 patients with CRC, homozygosity for the MLH1 -93A varian..." http://www.snpedia.com/index.php?title=Rs1800734 reference = Chr6 illumina rs1800750 31650942..31650942 "rs1800750, a SNP located at position -376 of the TNF gene, has been linked to increased risk for rec..." http://www.snpedia.com/index.php?title=Rs1800750 reference = Chr16 both rs1800775 55552737..55552737 "" http://www.snpedia.com/index.php?title=Rs1800775 reference = Chr4 snp rs1800787 155703465..155703465 "rs1800787(T;T) homozygotes are at 6 fold higher risk compared to (C;C) homozygotes or (C;T) heterozy..." http://www.snpedia.com/index.php?title=Rs1800787 reference = Chr7 affy rs1800795 22733170..22733170 "rs1800795 is a SNP in the promoter of the interleukin-6 IL6 gene, affecting the levels made of this ..." http://www.snpedia.com/index.php?title=Rs1800795 reference = Chr7 snp rs1800796 22732771..22732771 "rs1800796 IL-6 572G>C polymorphism (and h.211 haplotype) is associated with Abdominal Aortic Aneurys..." http://www.snpedia.com/index.php?title=Rs1800796 reference = Chr7 illumina rs1800797 22732746..22732746 "rs1800797, rs1800796 and rs1800795 have been shown to affect both the transcription and secretion of..." http://www.snpedia.com/index.php?title=Rs1800797 reference = Chr10 illumina rs1800858 42915974..42915974 "[omim:HIRSCHSPRUNG DISEASE]" http://www.snpedia.com/index.php?title=Rs1800858 reference = ChrNone snp rs1800865 2718271..2718271 "" http://www.snpedia.com/index.php?title=Rs1800865 reference = Chr5 illumina rs1800888 148187078..148187078 "[omim:BETA-2-ADRENORECEPTOR AGONIST, REDUCED RESPONSE TO]" http://www.snpedia.com/index.php?title=Rs1800888 reference = Chr1 illumina rs1800896 205013520..205013520 "Dust mite exposure modifies the effect of functional IL10 polymorphisms on allergy and asthma exacer..." http://www.snpedia.com/index.php?title=Rs1800896 reference = Chr5 snp rs1800925 132020708..132020708 "asthma related This SNP is in the promoter region of the IL-13 gene [http://www.ncbi.nlm.nih.gov/si..." http://www.snpedia.com/index.php?title=Rs1800925 reference = Chr1 snp rs1800947 157950062..157950062 "Although somewhat lacking in statistical power, several reports have linked rs1800947, a synonymous ..." http://www.snpedia.com/index.php?title=Rs1800947 reference = Chr11 snp rs1800955 626784..626784 "[http://originsgenomeresources.net/musings/?p=119 blog] ?쏞??allele of rs1800955 DRD4 gene survives a..." http://www.snpedia.com/index.php?title=Rs1800955 reference = Chr9 snp rs1800956 129626442..129626442 "rs1800956 (G/C transversion with D366H substitution) of endoglin may play an important role in the p..." http://www.snpedia.com/index.php?title=Rs1800956 reference = Chr8 snp rs1800972 6722833..6722833 "rs1800972(G;G) homozygotes appeared be at less risk (by a factor of 3.3, p=0.01) for Crohn's disease..." http://www.snpedia.com/index.php?title=Rs1800972 reference = Chr12 illumina rs1800974 54375624..54375624 "" http://www.snpedia.com/index.php?title=Rs1800974 reference = Chr9 illumina rs1800977 106730271..106730271 "The -14C->T polymorphism rs1800977 of the ABCA1 gene was significantly associated with atherothrombo..." http://www.snpedia.com/index.php?title=Rs1800977 reference = Chr3 snp rs1801019 125939432..125939432 "" http://www.snpedia.com/index.php?title=Rs1801019 reference = Chr11 snp rs1801028 112788694..112788694 "rs1801028 is a SNP in the dopamine D2 receptor DRD2 gene. A meta-analysis comprising 27 samples and ..." http://www.snpedia.com/index.php?title=Rs1801028 reference = Chr2 snp rs1801105 138593381..138593381 "asthma related [omim:ASTHMA, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1801105 reference = Chr1 both rs1801131 11777063..11777063 "rs1801131 is a SNP in the MTHFR gene, representing an A>C mutation at mRNA position 1298, resulting ..." http://www.snpedia.com/index.php?title=Rs1801131 reference = Chr1 illumina rs1801133 11778965..11778965 "rs1801133 is a SNP that is relatively common and has been studied for (relatively) a long time. Also..." http://www.snpedia.com/index.php?title=Rs1801133 reference = Chr10 affy rs1801157 44188263..44188263 "rs1801157(A) was associated with protection against infection (OR=0.63, P=0.01). In the MACS cohort,..." http://www.snpedia.com/index.php?title=Rs1801157 reference = Chr1 illumina rs1801159 97753983..97753983 "" http://www.snpedia.com/index.php?title=Rs1801159 reference = ChrX illumina rs1801187 32290917..32290917 "" http://www.snpedia.com/index.php?title=Rs1801187 reference = Chr22 illumina rs1801198 29341610..29341610 "[omim:TCN2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1801198 reference = Chr17 illumina rs1801200 35133114..35133114 "[omim:ERBB2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs1801200 reference = Chr4 both rs1801212 6353420..6353420 "" http://www.snpedia.com/index.php?title=Rs1801212 reference = Chr10 snp rs1801252 115794026..115794026 "Variation at this SNP, located in the ADRB1 gene, may encode either the amino acid serine or glycine..." http://www.snpedia.com/index.php?title=Rs1801252 reference = Chr10 snp rs1801253 115795046..115795046 "Variation at this SNP, located in the ADRB1 gene, may encode either the amino acid glycine or argini..." http://www.snpedia.com/index.php?title=Rs1801253 reference = Chr4 illumina rs1801260 55996126..55996126 "rs1801260, a SNP in the CLOCK gene known as 3111 T/C, has been reported to influence sleep and activ..." http://www.snpedia.com/index.php?title=Rs1801260 reference = Chr2 both rs1801262 182251700..182251700 "rs1801262 increases susceptibility to Type II Diabetes 1.15 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs1801262 reference = Chr1 illumina rs1801265 98121473..98121473 "[omim:DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs1801265 reference = Chr6 both rs1801270 36759949..36759949 "rs1801270 is a SNP known as p21 codon 31, although the gene now known to code for the p21 protein is..." http://www.snpedia.com/index.php?title=Rs1801270 reference = Chr16 both rs1801275 27281901..27281901 "[omim:ATOPY, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1801275 reference = Chr2 illumina rs1801278 227368788..227368788 "The INSR A-603G promoter rs1864010 SNP, which is located within a known Sp1-binding site, was associ..." http://www.snpedia.com/index.php?title=Rs1801278 reference = Chr8 illumina rs1801279 18301984..18301984 "rs1801279 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1801279 reference = Chr8 snp rs1801280 18302134..18302134 "rs1801280 is a SNP in the NAT2 gene, potentially encoding a variant detoxifying protein known as an ..." http://www.snpedia.com/index.php?title=Rs1801280 reference = Chr3 both rs1801282 12368125..12368125 "The association between type-1 diabetes and SNP rs1801282 is mentioned as being replicated in rs180..." http://www.snpedia.com/index.php?title=Rs1801282 reference = Chr6 affy rs1801334 161701215..161701215 "" http://www.snpedia.com/index.php?title=Rs1801334 reference = Chr15 both rs1801376 38265123..38265123 "" http://www.snpedia.com/index.php?title=Rs1801376 reference = Chr5 snp rs1801394 7923973..7923973 "rs1801394, also known as A22G or Ile22Met, is a SNP in the methionine synthase MTRR gene. This gene ..." http://www.snpedia.com/index.php?title=Rs1801394 reference = Chr13 illumina rs1801426 31870884..31870884 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs1801426 reference = Chr20 snp rs1801475 61508721..61508721 "" http://www.snpedia.com/index.php?title=Rs1801475 reference = Chr11 snp rs1801673 107680673..107680673 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs1801673 reference = Chr3 illumina rs1801725 123486447..123486447 "[omim:CALCIUM, SERUM LEVELS OF]" http://www.snpedia.com/index.php?title=Rs1801725 reference = Chr3 illumina rs1801726 123486522..123486522 "" http://www.snpedia.com/index.php?title=Rs1801726 reference = Chr8 both rs180223 133969434..133969434 "" http://www.snpedia.com/index.php?title=Rs180223 reference = Chr14 illumina rs1802710 100270398..100270398 "linked to brain tumors and lymphomas popular in pubmed" http://www.snpedia.com/index.php?title=Rs1802710 reference = Chr2 illumina rs1804020 71507683..71507683 "" http://www.snpedia.com/index.php?title=Rs1804020 reference = Chr5 snp rs1804197 112207808..112207808 "rs1804197, a SNP in the adenomatous polyposis of the colon APC gene, is associated with autism . Alt..." http://www.snpedia.com/index.php?title=Rs1804197 reference = ChrX both rs1804495 105165017..105165017 "[omim:THYROXINE-BINDING GLOBULIN, VARIANT P]" http://www.snpedia.com/index.php?title=Rs1804495 reference = Chr16 illumina rs1805005 88513345..88513345 "rs1805005, known as Val60Leu or V60L, is a SNP in the MC1R gene associated with light blond hair in ..." http://www.snpedia.com/index.php?title=Rs1805005 reference = Chr16 snp rs1805006 88513419..88513419 "rs1805006, known as Asp84Glu or D84E, is one of several SNPs in the MC1R gene associated with higher..." http://www.snpedia.com/index.php?title=Rs1805006 reference = Chr16 both rs1805007 88513618..88513618 "rs1805007, known as Arg151Cys or R151C, one of several SNPs in the MC1R gene associated with red hai..." http://www.snpedia.com/index.php?title=Rs1805007 reference = Chr16 illumina rs1805008 88513645..88513645 "rs1805008, known as Arg160Trp or R160W, is one of several SNPs in the MC1R gene associated with red ..." http://www.snpedia.com/index.php?title=Rs1805008 reference = Chr16 snp rs1805009 88514047..88514047 "rs1805009, known as Asp294His or D294H and located in the MC1R gene, is the most common variant asso..." http://www.snpedia.com/index.php?title=Rs1805009 reference = Chr6 both rs1805017 46792181..46792181 "" http://www.snpedia.com/index.php?title=Rs1805017 reference = Chr6 illumina rs1805018 46787262..46787262 "asthma related [omim:ASTHMA AND ATOPY, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1805018 reference = Chr18 illumina rs1805081 19394430..19394430 "" http://www.snpedia.com/index.php?title=Rs1805081 reference = Chr13 snp rs1805097 109233232..109233232 "[omim:DIABETES, TYPE II, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs1805097 reference = Chr22 affy rs1805129 27460458..27460458 "This SNP represents a silent polymorphism in the cancer-associated cell cycle regulator CHEK2 gene." http://www.snpedia.com/index.php?title=Rs1805129 reference = Chr2 illumina rs1805165 88656006..88656006 "" http://www.snpedia.com/index.php?title=Rs1805165 reference = Chr13 illumina rs1805388 107661592..107661592 "[omim:MULTIPLE MYELOMA, RESISTANCE TO]" http://www.snpedia.com/index.php?title=Rs1805388 reference = Chr13 snp rs1805389 107661610..107661610 "[omim:MULTIPLE MYELOMA, RESISTANCE TO]" http://www.snpedia.com/index.php?title=Rs1805389 reference = Chr12 snp rs1805762 8989169..8989169 "rs1805762, a SNP in the M6PR gene, was associated with risk for hypertension in a study involving 1,..." http://www.snpedia.com/index.php?title=Rs1805762 reference = Chr8 both rs1805874 91151238..91151238 "Parkinson's disease (PD). rs1805874 showed significance in both analyses (P = 7.1 x 10(-5); recessiv..." http://www.snpedia.com/index.php?title=Rs1805874 reference = Chr22 snp rs1807467 17285893..17285893 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs1807467 reference = Chr11 illumina rs1815739 66084671..66084671 "This SNP, in the ACTN3 gene, encodes a premature stop codon in a protein likely to be important in m..." http://www.snpedia.com/index.php?title=Rs1815739 reference = Chr5 affy rs1816071 160692534..160692534 "Located within intron 8 of the neurotransmitter type A gamma-aminobutyric acid (GABA) A receptor, be..." http://www.snpedia.com/index.php?title=Rs1816071 reference = Chr2 snp rs182549 136333224..136333224 "Also known as 'G/A(-22018)' and located in the MCM6 but with influence on the lactase LCT gene, rs18..." http://www.snpedia.com/index.php?title=Rs182549 reference = Chr16 snp rs183130 55548864..55548864 "The (C) allele of rs183130 was associated with risk for lower high-density lipoprotein (HDL) cholest..." http://www.snpedia.com/index.php?title=Rs183130 reference = Chr3 illumina rs1836915 156291796..156291796 "rs1836915 is a SNP in the membrane metalloendopeptidase MME gene, which is also known as CD10, CALLA..." http://www.snpedia.com/index.php?title=Rs1836915 reference = Chr7 snp rs1858830 116099675..116099675 "rs1858830, located in promoter of the MET gene, has been linked to a 2x increase in the risk of auti..." http://www.snpedia.com/index.php?title=Rs1858830 reference = Chr17 illumina rs1859962 66620348..66620348 "rs1859962 is a SNP on chromosome 17q24.3, associated with increased risk for prostate cancer in seve..." http://www.snpedia.com/index.php?title=Rs1859962 reference = Chr19 snp rs1864010 7245505..7245505 "The INSR A-603G promoter rs1864010 SNP, which is located within a known Sp1-binding site, was associ..." http://www.snpedia.com/index.php?title=Rs1864010 reference = Chr5 illumina rs1866388 142739978..142739978 "Associated with bone mineral density and thus osteoporosis in a Chinese population." http://www.snpedia.com/index.php?title=Rs1866388 reference = Chr1 snp rs1874792 22079822..22079822 "" http://www.snpedia.com/index.php?title=Rs1874792 reference = Chr17 snp rs1876828 41267306..41267306 "The G allele at the rs1876828 SNP was associated with lower z scores (P = .02) in males but tended t..." http://www.snpedia.com/index.php?title=Rs1876828 reference = Chr10 illumina rs1881747 54003581..54003581 "Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio..." http://www.snpedia.com/index.php?title=Rs1881747 reference = Chr20 illumina rs1883832 44180389..44180389 "Women with the TT genotype in rs1883832 had increased risk of osteopenia or osteoporosis. rs1883832..." http://www.snpedia.com/index.php?title=Rs1883832 reference = Chr20 snp rs1884613 42413829..42413829 "rs1884613 associated with type-2 diabetes in a Scandinavian population" http://www.snpedia.com/index.php?title=Rs1884613 reference = Chr20 affy rs1885120 33040650..33040650 "2,019 cases and 2,105 controls. Using pooling, we identified a new melanoma risk locus on chromosome..." http://www.snpedia.com/index.php?title=Rs1885120 reference = Chr17 illumina rs1889018 17675465..17675465 "rs1889018 is one of several SNPs associated with the SREBF1 gene that show a modest association with..." http://www.snpedia.com/index.php?title=Rs1889018 reference = Chr18 illumina rs1893217 12799340..12799340 "linked to Crohn's disease and type-1 diabetes" http://www.snpedia.com/index.php?title=Rs1893217 reference = Chr4 illumina rs1898830 154827903..154827903 "rs1898830, known as -15607A/G and located in the first intron of the TLR2 gene, is associated with a..." http://www.snpedia.com/index.php?title=Rs1898830 reference = Chr3 both rs1899951 12369840..12369840 "Associated with risk of lung cancer in a Chinese population" http://www.snpedia.com/index.php?title=Rs1899951 reference = Chr7 snp rs1922892 147207344..147207344 "Reported to be in very tight (r2>0.98) linkage with rs2710102, and thus potentially assoc..." http://www.snpedia.com/index.php?title=Rs1922892 reference = Chr9 affy rs1927911 119509875..119509875 "The rs1927911(T) allele was associated with a lower risk of nonfatal myocardial infarction (odds rat..." http://www.snpedia.com/index.php?title=Rs1927911 reference = Chr9 affy rs193008 107082627..107082627 "635 lung cancer cases with onset of disease below 51 years of age and 1,300 controls. major alleles ..." http://www.snpedia.com/index.php?title=Rs193008 reference = Chr1 illumina rs1930293 182560790..182560790 "rs1930293 increases susceptibility to Prostate cancer 1.20 times for heterozygotes (AG) and 1.70 tim..." http://www.snpedia.com/index.php?title=Rs1930293 reference = Chr9 affy rs1930780 122726040..122726040 "rs1930780 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumato..." http://www.snpedia.com/index.php?title=Rs1930780 reference = Chr6 affy rs1934328 45573731..45573731 "rs910586, rs2819861, and rs1934328 may influence cleft palate" http://www.snpedia.com/index.php?title=Rs1934328 reference = Chr10 both rs1934951 96788538..96788538 "(T;T) associated with a higher risk of osteonecrosis of the jaw in am small study of multiple myelom..." http://www.snpedia.com/index.php?title=Rs1934951 reference = Chr1 illumina rs1935881 188333009..188333009 "Left atrial size, rs1935881 (FAM5C, p = 6.56*10(-6));" http://www.snpedia.com/index.php?title=Rs1935881 reference = Chr13 affy rs1937506 66933372..66933372 "rs1937506 has been reported in a large study to be associated with high blood pressure. The risk all..." http://www.snpedia.com/index.php?title=Rs1937506 reference = Chr10 illumina rs1937845 5126148..5126148 "rs1937845 minor allele seems slightly protective against cancer in 1,150 cases of urothelial carcino..." http://www.snpedia.com/index.php?title=Rs1937845 reference = Chr11 snp rs1938901 102166875..102166875 "635 lung cancer cases with onset of disease below 51 years of age and 1,300 controls. major alleles ..." http://www.snpedia.com/index.php?title=Rs1938901 reference = Chr11 illumina rs1946518 111540668..111540668 "rs1946518 and rs1946519 may influence cervical cancer" http://www.snpedia.com/index.php?title=Rs1946518 reference = Chr11 illumina rs1946519 111540717..111540717 "rs1946518 and rs1946519 may influence cervical cancer" http://www.snpedia.com/index.php?title=Rs1946519 reference = Chr15 illumina rs1948 76704454..76704454 "The (C;C) genotype (as published) of rs1948 was calculated to represent a hazard ratio of 1.29 (CI: ..." http://www.snpedia.com/index.php?title=Rs1948 reference = Chr14 illumina rs1950902 63952133..63952133 "" http://www.snpedia.com/index.php?title=Rs1950902 reference = Chr14 snp rs1950952 38847427..38847427 "" http://www.snpedia.com/index.php?title=Rs1950952 reference = Chr9 illumina rs1953126 122680321..122680321 "A study of 475 Caucasian patients concluded that rs1953126, on chromosome 9q33.2, was significantly ..." http://www.snpedia.com/index.php?title=Rs1953126 reference = Chr11 illumina rs1954787 120168573..120168573 "rs1954787, located in an intron of the HTR2A gene, was found to be associated with a somewhat increa..." http://www.snpedia.com/index.php?title=Rs1954787 reference = Chr1 illumina rs197414 112110646..112110646 "The homozygous was associated with a significantly increased bladder cancer risk [odds ratios (OR), ..." http://www.snpedia.com/index.php?title=Rs197414 reference = Chr9 both rs1975197 8836955..8836955 "rs1975197, a SNP in the motor neuron PTPRD gene, has been linked to restless legs syndrome based on ..." http://www.snpedia.com/index.php?title=Rs1975197 reference = Chr19 snp rs1978237 5160641..5160641 "rs1143699, rs4807015, and rs1978237 confer an increased risk of developing type-2 diabetes" http://www.snpedia.com/index.php?title=Rs1978237 reference = Chr12 illumina rs1978331 94933332..94933332 "rs1978331 is one of several SNPs associated with asthma and allergy susceptibility based on a study ..." http://www.snpedia.com/index.php?title=Rs1978331 reference = ChrX affy rs1980459 142179559..142179559 "" http://www.snpedia.com/index.php?title=Rs1980459 reference = Chr19 snp rs1982073 46550761..46550761 "rs1982073, also known as codon 10, +10T/C or T869C, a SNP in the first exon of the transforming grow..." http://www.snpedia.com/index.php?title=Rs1982073 reference = Chr12 snp rs1982526 130805495..130805495 "This SNP is part of a haplotype reported for the KLRK1 gene, potentially associated with risk for co..." http://www.snpedia.com/index.php?title=Rs1982526 reference = Chr1 illumina rs198389 11841858..11841858 "Brain natriuretic peptide (BNP) has been widely used for the diagnosis and prognostic evaluation of ..." http://www.snpedia.com/index.php?title=Rs198389 reference = Chr2 illumina rs1990760 162832297..162832297 "[http://jcem.endojournals.org/cgi/content/abstract/92/8/3338 Abstract] associated with type-1 diabet..." http://www.snpedia.com/index.php?title=Rs1990760 reference = Chr14 snp rs1991517 80680336..80680336 "" http://www.snpedia.com/index.php?title=Rs1991517 reference = Chr5 snp rs1992660 40450824..40450824 "rs1992660 is a SNP upstream of the PTGER4 gene that was found in a genome-wide association study to ..." http://www.snpedia.com/index.php?title=Rs1992660 reference = Chr5 snp rs1992662 40429609..40429609 "rs1992662 is a SNP upstream of the PTGER4 gene that was found in a genome-wide association study to ..." http://www.snpedia.com/index.php?title=Rs1992662 reference = Chr6 illumina rs1999805 152110057..152110057 "rs1999805 increases susceptibility to Bone mineral density variations, lower for carriers of the A a..." http://www.snpedia.com/index.php?title=Rs1999805 reference = Chr22 snp rs2003813 34958939..34958939 "rs9610449 schizophrenia (377 families, 1161 genotyped members and 647 genotyped affected in total) r..." http://www.snpedia.com/index.php?title=Rs2003813 reference = Chr7 snp rs2004640 128365537..128365537 "rs2004640, a SNP in the IRF5 gene in chromosomal region 7q32.1, is one of several SNPs associated wi..." http://www.snpedia.com/index.php?title=Rs2004640 reference = Chr22 snp rs2008720 17303745..17303745 "" http://www.snpedia.com/index.php?title=Rs2008720 reference = Chr5 affy rs2011077 176454062..176454062 "A study of ~500 Japanese prostate cancer patients found that individuals with a rs2011077(G;G) genot..." http://www.snpedia.com/index.php?title=Rs2011077 reference = Chr10 illumina rs2014307 124207622..124207622 "[http://7thspace.com/headlines/283954/the_neincbi_dbgap_database_genotypes_and_haplotypes_that_may_p..." http://www.snpedia.com/index.php?title=Rs2014307 reference = Chr1 snp rs2015352 16243654..16243654 "" http://www.snpedia.com/index.php?title=Rs2015352 reference = Chr6 illumina rs2016520 35486756..35486756 "Associated with baseline cholesterol levels in a study of 9,000+ individuals in Washington County, M..." http://www.snpedia.com/index.php?title=Rs2016520 reference = ChrNone snp rs2020857 13540146..13540146 "" http://www.snpedia.com/index.php?title=Rs2020857 reference = Chr2 snp rs2020908 47879812..47879812 "" http://www.snpedia.com/index.php?title=Rs2020908 reference = Chr9 illumina rs2020927 106593006..106593006 "rs2297404, rs2230808, and rs2020927 haplotype (CAC) was more prevalent in the Alzheimer's disease gr..." http://www.snpedia.com/index.php?title=Rs2020927 reference = Chr13 affy rs2031640 22828055..22828055 "" http://www.snpedia.com/index.php?title=Rs2031640 reference = ChrNone illumina rs20320 13407557..13407557 "" http://www.snpedia.com/index.php?title=Rs20320 reference = ChrNone illumina rs20321 13411808..13411808 "" http://www.snpedia.com/index.php?title=Rs20321 reference = Chr7 illumina rs2032582 86998554..86998554 "rs2032582, also known as G2677T, is a nonsynonymous SNP located in exon 21 of the ABCB1 gene. G2677 ..." http://www.snpedia.com/index.php?title=Rs2032582 reference = Chr7 illumina rs2032583 86998497..86998497 "rs2032583 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs2032583 reference = ChrNone snp rs2032589 13540504..13540504 "" http://www.snpedia.com/index.php?title=Rs2032589 reference = ChrNone illumina rs2032590 13529007..13529007 "" http://www.snpedia.com/index.php?title=Rs2032590 reference = ChrNone affy rs2032591 13540076..13540076 "" http://www.snpedia.com/index.php?title=Rs2032591 reference = ChrNone affy rs2032593 13540810..13540810 "" http://www.snpedia.com/index.php?title=Rs2032593 reference = ChrNone illumina rs2032594 13323111..13323111 "" http://www.snpedia.com/index.php?title=Rs2032594 reference = ChrNone affy rs2032595 13323385..13323385 "" http://www.snpedia.com/index.php?title=Rs2032595 reference = ChrNone affy rs2032596 13348094..13348094 "" http://www.snpedia.com/index.php?title=Rs2032596 reference = ChrNone illumina rs2032597 13357186..13357186 "This SNP also goes under the name [http://isogg.org/tree/ISOGG_YDNA_SNP_Index08.html M170]. As such,..." http://www.snpedia.com/index.php?title=Rs2032597 reference = ChrNone both rs2032598 13359735..13359735 "" http://www.snpedia.com/index.php?title=Rs2032598 reference = ChrNone snp rs2032599 13360948..13360948 "" http://www.snpedia.com/index.php?title=Rs2032599 reference = ChrNone both rs2032600 13398177..13398177 "" http://www.snpedia.com/index.php?title=Rs2032600 reference = ChrNone illumina rs2032601 13378470..13378470 "" http://www.snpedia.com/index.php?title=Rs2032601 reference = ChrNone snp rs2032602 13463674..13463674 "This SNP also goes under the name [http://isogg.org/tree/ISOGG_YDNA_SNP_Index08.html M174]. As such,..." http://www.snpedia.com/index.php?title=Rs2032602 reference = ChrNone illumina rs2032603 13477921..13477921 "" http://www.snpedia.com/index.php?title=Rs2032603 reference = ChrNone illumina rs2032604 13479028..13479028 "" http://www.snpedia.com/index.php?title=Rs2032604 reference = ChrNone affy rs2032605 13434263..13434263 "" http://www.snpedia.com/index.php?title=Rs2032605 reference = ChrNone snp rs2032606 13455099..13455099 "" http://www.snpedia.com/index.php?title=Rs2032606 reference = ChrNone illumina rs2032607 13414253..13414253 "" http://www.snpedia.com/index.php?title=Rs2032607 reference = ChrY affy rs2032608 20385500..20385500 "" http://www.snpedia.com/index.php?title=Rs2032608 reference = ChrY snp rs2032609 20395526..20395526 "" http://www.snpedia.com/index.php?title=Rs2032609 reference = ChrNone affy rs2032610 13534992..13534992 "" http://www.snpedia.com/index.php?title=Rs2032610 reference = ChrY snp rs2032611 20325812..20325812 "" http://www.snpedia.com/index.php?title=Rs2032611 reference = ChrY illumina rs2032612 20325879..20325879 "" http://www.snpedia.com/index.php?title=Rs2032612 reference = ChrY illumina rs2032613 20391026..20391026 "" http://www.snpedia.com/index.php?title=Rs2032613 reference = ChrY snp rs2032614 20389675..20389675 "" http://www.snpedia.com/index.php?title=Rs2032614 reference = ChrY snp rs2032615 20389651..20389651 "" http://www.snpedia.com/index.php?title=Rs2032615 reference = ChrY snp rs2032616 20355604..20355604 "" http://www.snpedia.com/index.php?title=Rs2032616 reference = ChrY illumina rs2032617 20355649..20355649 "" http://www.snpedia.com/index.php?title=Rs2032617 reference = ChrY snp rs2032618 20353141..20353141 "" http://www.snpedia.com/index.php?title=Rs2032618 reference = ChrY affy rs2032619 20384888..20384888 "" http://www.snpedia.com/index.php?title=Rs2032619 reference = ChrY affy rs2032620 20328652..20328652 "" http://www.snpedia.com/index.php?title=Rs2032620 reference = ChrY both rs2032621 20332126..20332126 "" http://www.snpedia.com/index.php?title=Rs2032621 reference = ChrY affy rs2032622 20332274..20332274 "" http://www.snpedia.com/index.php?title=Rs2032622 reference = ChrY snp rs2032623 20337460..20337460 "" http://www.snpedia.com/index.php?title=Rs2032623 reference = ChrNone both rs2032624 13535818..13535818 "" http://www.snpedia.com/index.php?title=Rs2032624 reference = ChrY affy rs2032625 20330026..20330026 "" http://www.snpedia.com/index.php?title=Rs2032625 reference = ChrY snp rs2032626 20362771..20362771 "" http://www.snpedia.com/index.php?title=Rs2032626 reference = ChrY both rs2032627 20340961..20340961 "" http://www.snpedia.com/index.php?title=Rs2032627 reference = ChrY snp rs2032628 20338197..20338197 "" http://www.snpedia.com/index.php?title=Rs2032628 reference = ChrY illumina rs2032629 20325209..20325209 "" http://www.snpedia.com/index.php?title=Rs2032629 reference = ChrY snp rs2032630 20326228..20326228 "" http://www.snpedia.com/index.php?title=Rs2032630 reference = ChrY affy rs2032631 20327175..20327175 "" http://www.snpedia.com/index.php?title=Rs2032631 reference = ChrY snp rs2032632 20328060..20328060 "" http://www.snpedia.com/index.php?title=Rs2032632 reference = ChrY snp rs2032633 20328114..20328114 "" http://www.snpedia.com/index.php?title=Rs2032633 reference = ChrY snp rs2032634 20348262..20348262 "" http://www.snpedia.com/index.php?title=Rs2032634 reference = ChrY snp rs2032635 20349155..20349155 "" http://www.snpedia.com/index.php?title=Rs2032635 reference = ChrNone affy rs2032636 13536923..13536923 "" http://www.snpedia.com/index.php?title=Rs2032636 reference = ChrY illumina rs2032637 20353795..20353795 "" http://www.snpedia.com/index.php?title=Rs2032637 reference = ChrY snp rs2032638 20353835..20353835 "" http://www.snpedia.com/index.php?title=Rs2032638 reference = ChrY snp rs2032639 20349565..20349565 "" http://www.snpedia.com/index.php?title=Rs2032639 reference = ChrY illumina rs2032640 20351960..20351960 "" http://www.snpedia.com/index.php?title=Rs2032640 reference = ChrY snp rs2032641 20332675..20332675 "" http://www.snpedia.com/index.php?title=Rs2032641 reference = ChrY snp rs2032642 20357751..20357751 "" http://www.snpedia.com/index.php?title=Rs2032642 reference = ChrY illumina rs2032643 20365305..20365305 "" http://www.snpedia.com/index.php?title=Rs2032643 reference = ChrY illumina rs2032644 20365497..20365497 "" http://www.snpedia.com/index.php?title=Rs2032644 reference = ChrY affy rs2032645 20360237..20360237 "" http://www.snpedia.com/index.php?title=Rs2032645 reference = ChrY snp rs2032646 20383717..20383717 "" http://www.snpedia.com/index.php?title=Rs2032646 reference = ChrY snp rs2032647 20397546..20397546 "" http://www.snpedia.com/index.php?title=Rs2032647 reference = ChrY illumina rs2032648 20363411..20363411 "" http://www.snpedia.com/index.php?title=Rs2032648 reference = ChrNone snp rs2032649 13538886..13538886 "" http://www.snpedia.com/index.php?title=Rs2032649 reference = ChrY snp rs2032650 20397832..20397832 "" http://www.snpedia.com/index.php?title=Rs2032650 reference = ChrY snp rs2032651 20366926..20366926 "" http://www.snpedia.com/index.php?title=Rs2032651 reference = ChrY both rs2032652 20376701..20376701 "" http://www.snpedia.com/index.php?title=Rs2032652 reference = ChrNone affy rs2032653 14100931..14100931 "" http://www.snpedia.com/index.php?title=Rs2032653 reference = ChrNone affy rs2032654 13977218..13977218 "" http://www.snpedia.com/index.php?title=Rs2032654 reference = ChrNone snp rs2032655 14100595..14100595 "" http://www.snpedia.com/index.php?title=Rs2032655 reference = ChrNone snp rs2032656 14096856..14096856 "" http://www.snpedia.com/index.php?title=Rs2032656 reference = ChrNone snp rs2032657 14096903..14096903 "" http://www.snpedia.com/index.php?title=Rs2032657 reference = ChrNone snp rs2032658 14091377..14091377 "" http://www.snpedia.com/index.php?title=Rs2032658 reference = ChrNone illumina rs2032659 14085597..14085597 "" http://www.snpedia.com/index.php?title=Rs2032659 reference = ChrNone snp rs2032660 14085174..14085174 "" http://www.snpedia.com/index.php?title=Rs2032660 reference = ChrNone snp rs2032661 14085184..14085184 "" http://www.snpedia.com/index.php?title=Rs2032661 reference = ChrNone snp rs2032662 13523656..13523656 "" http://www.snpedia.com/index.php?title=Rs2032662 reference = ChrNone both rs2032663 14054008..14054008 "" http://www.snpedia.com/index.php?title=Rs2032663 reference = ChrNone illumina rs2032664 14036089..14036089 "" http://www.snpedia.com/index.php?title=Rs2032664 reference = ChrNone both rs2032665 14036145..14036145 "" http://www.snpedia.com/index.php?title=Rs2032665 reference = ChrNone both rs2032666 13946958..13946958 "" http://www.snpedia.com/index.php?title=Rs2032666 reference = ChrNone illumina rs2032667 13945710..13945710 "" http://www.snpedia.com/index.php?title=Rs2032667 reference = ChrNone illumina rs2032668 13946727..13946727 "" http://www.snpedia.com/index.php?title=Rs2032668 reference = ChrNone illumina rs2032669 13946309..13946309 "" http://www.snpedia.com/index.php?title=Rs2032669 reference = ChrNone snp rs2032670 13946444..13946444 "" http://www.snpedia.com/index.php?title=Rs2032670 reference = ChrNone illumina rs2032671 13946457..13946457 "" http://www.snpedia.com/index.php?title=Rs2032671 reference = ChrY affy rs2032672 20353269..20353269 "" http://www.snpedia.com/index.php?title=Rs2032672 reference = ChrY affy rs2032673 20353446..20353446 "" http://www.snpedia.com/index.php?title=Rs2032673 reference = ChrNone snp rs2032674 13981319..13981319 "" http://www.snpedia.com/index.php?title=Rs2032674 reference = ChrY snp rs2032675 20353562..20353562 "" http://www.snpedia.com/index.php?title=Rs2032675 reference = ChrNone snp rs2032676 13523899..13523899 "" http://www.snpedia.com/index.php?title=Rs2032676 reference = ChrNone illumina rs2032677 13523944..13523944 "" http://www.snpedia.com/index.php?title=Rs2032677 reference = ChrNone snp rs2032678 14018100..14018100 "" http://www.snpedia.com/index.php?title=Rs2032678 reference = ChrY snp rs2032679 20392323..20392323 "" http://www.snpedia.com/index.php?title=Rs2032679 reference = ChrNone snp rs2032680 13525930..13525930 "" http://www.snpedia.com/index.php?title=Rs2032680 reference = ChrNone snp rs2032681 13432855..13432855 "" http://www.snpedia.com/index.php?title=Rs2032681 reference = Chr17 illumina rs203462 19753133..19753133 "Linked to breast cancer [omim:LONGEVITY, REDUCED]" http://www.snpedia.com/index.php?title=Rs203462 reference = ChrNone snp rs2040410 32710676..32710676 "People with the human leukocyte antigen (HLA) genotype DRB1*0301-DQA1*0501-DQB1*0201/DRB1*04-DQA1*03..." http://www.snpedia.com/index.php?title=Rs2040410 reference = Chr7 illumina rs2040639 152006121..152006121 "18067C>T possibly related to non-Hodgkin lymphoma rs2040639-AG, contribute to oral cancer risk. pseu..." http://www.snpedia.com/index.php?title=Rs2040639 reference = Chr1 snp rs20417 184916944..184916944 "In a group of Pima Indians, individuals with the variant PTGS2 rs20417 CC genotype had a 30% higher ..." http://www.snpedia.com/index.php?title=Rs20417 reference = Chr10 both rs2043556 52729412..52729412 "" http://www.snpedia.com/index.php?title=Rs2043556 reference = Chr6 both rs20455 39433056..39433056 "rs20455, often called Arg719, is a reasonably well studied SNP in the KIF6 gene. The risk allele (en..." http://www.snpedia.com/index.php?title=Rs20455 reference = Chr11 snp rs2049045 27650817..27650817 "Alzheimer's disease risk for non ApoE4 carriers is affected by the heterozygous form of rs6265, as w..." http://www.snpedia.com/index.php?title=Rs2049045 reference = Chr14 both rs2053149 65850316..65850316 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs2053149 reference = Chr2 snp rs2053724 116227287..116227287 "" http://www.snpedia.com/index.php?title=Rs2053724 reference = Chr5 both rs20541 132023863..132023863 "rs20541 influences the effect of maternal smoking during pregnancy and persistent childhood asthma" http://www.snpedia.com/index.php?title=Rs20541 reference = Chr22 illumina rs20551 39877954..39877954 "" http://www.snpedia.com/index.php?title=Rs20551 reference = Chr4 affy rs2056116 12619085..12619085 "rs2056116 is a somewhat unusual SNP, in that it is from an 'ultraconserved element' of the genome, m..." http://www.snpedia.com/index.php?title=Rs2056116 reference = Chr8 illumina rs20576 23114165..23114165 "Carriers of an 228Ala allele for rs20576 who have prostate cancer and are treated by radiation thera..." http://www.snpedia.com/index.php?title=Rs20576 reference = Chr2 illumina rs2059693 220150734..220150734 "A study of 577 cases of testicular germ cell tumors, the most common testicular cancer in young men,..." http://www.snpedia.com/index.php?title=Rs2059693 reference = Chr6 snp rs2064318 35585003..35585003 "" http://www.snpedia.com/index.php?title=Rs2064318 reference = Chr1 illumina rs2066470 11785644..11785644 "Associated with lean body mass but not fat body mass in a study of ~1,800 Caucasians" http://www.snpedia.com/index.php?title=Rs2066470 reference = Chr4 affy rs2066702 100448040..100448040 "this [http://hmg.oxfordjournals.org/cgi/content/full/15/9/1539 paper] found significant association ..." http://www.snpedia.com/index.php?title=Rs2066702 reference = Chr16 both rs2066843 49302700..49302700 "rs2066843 increases susceptibility to Crohn's disease 4.09 times for carriers of the T allele [PMID ..." http://www.snpedia.com/index.php?title=Rs2066843 reference = Chr16 illumina rs2066844 49303427..49303427 "rs2066844 is mentioned in as being strongly associated with Crohn's disease [omim:CROHN DISEASE, S..." http://www.snpedia.com/index.php?title=Rs2066844 reference = Chr16 snp rs2066845 49314041..49314041 "rs2066845, a SNP in the NOD2 gene, has been linked to Crohn's disease. rs2066845 has also been repo..." http://www.snpedia.com/index.php?title=Rs2066845 reference = Chr16 snp rs2066847 49321279..49321279 "linked to Crohn's disease. it is the same snp as rs5743293" http://www.snpedia.com/index.php?title=Rs2066847 reference = Chr7 both rs2066853 17345635..17345635 "rs2066853 has been associated with increased risk for colorectal polyps depending on the amount of m..." http://www.snpedia.com/index.php?title=Rs2066853 reference = Chr7 both rs2066992 22734774..22734774 "rs2066992 coronary artery disease 190 affected Asian Indian sibling pairs" http://www.snpedia.com/index.php?title=Rs2066992 reference = ChrY snp rs2068150 17348769..17348769 "" http://www.snpedia.com/index.php?title=Rs2068150 reference = Chr7 snp rs2069442 150386138..150386138 "(G;G) showed a 1.9-fold increased risk of Alzheimer's disease (95 % CI 1.16-3.10, p = 0.003)" http://www.snpedia.com/index.php?title=Rs2069442 reference = Chr8 both rs2069556 133989700..133989700 "" http://www.snpedia.com/index.php?title=Rs2069556 reference = Chr8 illumina rs2069561 134044465..134044465 "" http://www.snpedia.com/index.php?title=Rs2069561 reference = Chr12 affy rs2069705 66841278..66841278 "Associated with at least one 'mortality outcome' in a study of ~10,000 individuals." http://www.snpedia.com/index.php?title=Rs2069705 reference = Chr7 illumina rs2069830 22733662..22733662 "stroke rs2069830(T) (frequency = 5%) protective among non-smokers (OR = 0.30, 95% CI=0.11-.082, p=0...." http://www.snpedia.com/index.php?title=Rs2069830 reference = Chr7 illumina rs2069832 22733958..22733958 "[http://7thspace.com/headlines/291555/ischemic_stroke_risk_smoking_and_the_genetics_of_inflammation_..." http://www.snpedia.com/index.php?title=Rs2069832 reference = Chr2 snp rs2069912 127894661..127894661 "The rs2069912(C) allele is associated with severe sepsis and thus increased risk of death and organ ..." http://www.snpedia.com/index.php?title=Rs2069912 reference = Chr11 illumina rs2070045 120953300..120953300 "SNP rs2070045, a variant of the SORL1 gene, has been reported to be associated with Alzheimer's dise..." http://www.snpedia.com/index.php?title=Rs2070045 reference = Chr9 snp rs2070075 34638418..34638418 "[omim:LOS ANGELES VARIANT]" http://www.snpedia.com/index.php?title=Rs2070075 reference = Chr17 illumina rs2070106 37379390..37379390 "rs2070106 was potentially associated with schizophrenia (P=0.027) in a Caucasian population." http://www.snpedia.com/index.php?title=Rs2070106 reference = Chr12 illumina rs2070739 46654243..46654243 "" http://www.snpedia.com/index.php?title=Rs2070739 reference = Chr11 illumina rs2070762 2142911..2142911 "association with essential hypertension . Functional analysis showed that the C allele of rs2070762 ..." http://www.snpedia.com/index.php?title=Rs2070762 reference = Chr17 illumina rs2070863 1595252..1595252 "" http://www.snpedia.com/index.php?title=Rs2070863 reference = Chr5 illumina rs2070874 132037609..132037609 "Visceral leishmaniasis (VL) caused by Leishmania chagasi is endemic to northeast Brazil. A positive ..." http://www.snpedia.com/index.php?title=Rs2070874 reference = Chr21 affy rs2070947 45165271..45165271 "" http://www.snpedia.com/index.php?title=Rs2070947 reference = Chr20 snp rs2071023 55569340..55569340 "rs2071023 increases susceptibility to Type II Diabetes 1.27 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs2071023 reference = Chr21 illumina rs2071152 44327549..44327549 "" http://www.snpedia.com/index.php?title=Rs2071152 reference = Chr7 illumina rs2071307 73108650..73108650 "" http://www.snpedia.com/index.php?title=Rs2071307 reference = Chr22 illumina rs2071421 49411282..49411282 "[omim:ARYLSULFATASE A POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs2071421 reference = Chr1 snp rs2072493 221351222..221351222 "[omim:LEGIONNAIRE DISEASE, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs2072493 reference = Chr22 both rs2072797 37464153..37464153 "rs2072797, a SNP in the UNC84B gene also known as G671S, is associated with risk for developing Non-..." http://www.snpedia.com/index.php?title=Rs2072797 reference = Chr14 illumina rs2073342 20430056..20430056 "" http://www.snpedia.com/index.php?title=Rs2073342 reference = Chr14 illumina rs2073347 50293539..50293539 "" http://www.snpedia.com/index.php?title=Rs2073347 reference = Chr1 snp rs2073658 159277386..159277386 "rs2073658 a borderline association with metabolic syndrome was observed (p = 0.036, IDF), the minor ..." http://www.snpedia.com/index.php?title=Rs2073658 reference = Chr15 both rs2073711 63281265..63281265 "A study of Asian patients with lumbar disc disease (LDD) implicates each copy of a (C) allele of SNP..." http://www.snpedia.com/index.php?title=Rs2073711 reference = Chr22 illumina rs2073748 18348971..18348971 "" http://www.snpedia.com/index.php?title=Rs2073748 reference = Chr5 illumina rs2073838 131677121..131677121 "rs2073838 and rs3792876 replicated for rheumatoid arthritis in Japanese, but not Caucasian populatio..." http://www.snpedia.com/index.php?title=Rs2073838 reference = Chr17 illumina rs2074190 43166209..43166209 "rs2074190(G;G) and rs2074190(A;G) genotypes for the TBX21 gene are calculated to be at 2.19 fold hig..." http://www.snpedia.com/index.php?title=Rs2074190 reference = ChrY both rs2075181 7606726..7606726 "" http://www.snpedia.com/index.php?title=Rs2075181 reference = Chr11 illumina rs2075291 116166602..116166602 "SNP rs2075291 represents a glycine to cysteine substitution at amino acid 185 of the APOA5 protein; ..." http://www.snpedia.com/index.php?title=Rs2075291 reference = Chr5 illumina rs2075685 82408421..82408421 "18067C>T possibly related to non-Hodgkin lymphoma rs2040639-AG, contribute to oral cancer risk. pseu..." http://www.snpedia.com/index.php?title=Rs2075685 reference = Chr6 both rs2076530 32471794..32471794 "rs2076530(A) was estimated to double the risk of developing sarcoidosis, at least as based on a stud..." http://www.snpedia.com/index.php?title=Rs2076530 reference = Chr16 both rs2076756 49314382..49314382 "rs2076756 is a SNP of the NOD2 gene found in a genome-wide association study to be associated with C..." http://www.snpedia.com/index.php?title=Rs2076756 reference = Chr3 snp rs2077119 187813156..187813156 "rs2077119, also known as -469T/G, is a SNP in the alpha-2-HS-glycoprotein AHSG gene. In a study of ~..." http://www.snpedia.com/index.php?title=Rs2077119 reference = Chr10 both rs2104286 6139051..6139051 "rs2104286 has also been reported in a large study to be associated with type-1 diabetes. The risk al..." http://www.snpedia.com/index.php?title=Rs2104286 reference = Chr12 both rs2107301 46541837..46541837 "rs2107301 is a SNP in the vitamin D VDR receptor gene. rs2107301(T;T) homozygotes were associated wi..." http://www.snpedia.com/index.php?title=Rs2107301 reference = Chr17 illumina rs2107538 31231893..31231893 "discussed in the [http://spittoon.23andme.com/2008/07/16/snpwatch-genetic-variant-common-in-african-..." http://www.snpedia.com/index.php?title=Rs2107538 reference = Chr7 illumina rs2107732 45044503..45044503 "" http://www.snpedia.com/index.php?title=Rs2107732 reference = Chr11 affy rs211105 18011880..18011880 "rs211105, rs1800532 and rs7933505 related to schizophrenia" http://www.snpedia.com/index.php?title=Rs211105 reference = Chr13 snp rs211239 32494189..32494189 "rs211239 is one of 2 SNPs (the other is rs2249358) in the KLOTHO gene found in a study of ~150 sickl..." http://www.snpedia.com/index.php?title=Rs211239 reference = Chr8 snp rs2114358 129090361..129090361 "" http://www.snpedia.com/index.php?title=Rs2114358 reference = Chr8 affy rs2119783 58104912..58104912 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs2119783 reference = Chr10 illumina rs2135720 55425497..55425497 "" http://www.snpedia.com/index.php?title=Rs2135720 reference = Chr7 illumina rs213950 116986769..116986769 "rs213950, a SNP in the cystic fibrosis CFTR gene, has been reported in a large study to be associate..." http://www.snpedia.com/index.php?title=Rs213950 reference = Chr6 snp rs2143340 24767050..24767050 "Rs2143340, a SNP in the TTRAP gene, is in a region that crops up in several independent studies as l..." http://www.snpedia.com/index.php?title=Rs2143340 reference = Chr20 illumina rs2144908 42419131..42419131 "1. effects type-2 diabetes 2. pmids15047633 15504983 15735892 16522129 16522130 16523192 16523193 16..." http://www.snpedia.com/index.php?title=Rs2144908 reference = Chr6 snp rs2146323 43853073..43853073 "[http://originsgenomeresources.net/musings/?p=171 origins blog] rs833070 and rs2146323. Individuals ..." http://www.snpedia.com/index.php?title=Rs2146323 reference = Chr6 affy rs2152750 152111838..152111838 "rs2152750 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone min..." http://www.snpedia.com/index.php?title=Rs2152750 reference = Chr22 illumina rs2156921 21899063..21899063 "rs2156921, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs2156921 reference = Chr22 illumina rs2157249 34960985..34960985 "rs9610449 schizophrenia (377 families, 1161 genotyped members and 647 genotyped affected in total) r..." http://www.snpedia.com/index.php?title=Rs2157249 reference = Chr12 illumina rs2159100 2216654..2216654 "[http://spittoon.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-..." http://www.snpedia.com/index.php?title=Rs2159100 reference = Chr12 both rs2160525 12161557..12161557 "rs2160525 is in linkage disequilibrium with a polymorphism that increases susceptibility to Alzheime..." http://www.snpedia.com/index.php?title=Rs2160525 reference = Chr12 illumina rs216321 6014245..6014245 "" http://www.snpedia.com/index.php?title=Rs216321 reference = ChrNone both rs2165241 72009255..72009255 "This SNP, located in an intron of the LOXL1 gene, was initially reported to be associated with exfol..." http://www.snpedia.com/index.php?title=Rs2165241 reference = Chr7 both rs2167270 127668585..127668585 "rs2167270 is a SNP in the leptin LEP gene. In a study of ~1,500 colon cancer patients, the rs2167270..." http://www.snpedia.com/index.php?title=Rs2167270 reference = Chr11 illumina rs217086 87685231..87685231 "" http://www.snpedia.com/index.php?title=Rs217086 reference = Chr3 illumina rs2172397 81725857..81725857 "" http://www.snpedia.com/index.php?title=Rs2172397 reference = Chr6 snp rs2179922 152338793..152338793 "A study of 1153 elderly Swedish men (age 70) concluded that rs2179922(G;G) homozygotes were between ..." http://www.snpedia.com/index.php?title=Rs2179922 reference = Chr9 both rs2184026 100344169..100344169 "Associated with nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs2184026 reference = Chr6 both rs2187668 32713862..32713862 "In at least UK populations, and perhaps others, SNP rs2187668 is a tag SNP for the HLA-DRB1*0301 all..." http://www.snpedia.com/index.php?title=Rs2187668 reference = Chr7 snp rs2190004 146899393..146899393 "" http://www.snpedia.com/index.php?title=Rs2190004 reference = Chr2 illumina rs2193225 50932986..50932986 "rs2193225 has been reported to be associated with increased risk for nicotine dependence." http://www.snpedia.com/index.php?title=Rs2193225 reference = ChrY illumina rs2196155 21074650..21074650 "" http://www.snpedia.com/index.php?title=Rs2196155 reference = Chr3 illumina rs2197423 12366583..12366583 "associated with type-2 diabetes" http://www.snpedia.com/index.php?title=Rs2197423 reference = Chr4 both rs2200733 111929618..111929618 "Two SNPs from chromosome 4q25, rs2200733 and rs10033464, were found to be associated with atrial fib..." http://www.snpedia.com/index.php?title=Rs2200733 reference = Chr1 both rs2201841 67466790..67466790 "SNP rs2201841, in the IL23R gene, is associated with increased risk for Crohn's disease in both Jewi..." http://www.snpedia.com/index.php?title=Rs2201841 reference = Chr10 snp rs2209972 94169008..94169008 "rs2209972, a SNP associated with the insulin-degrading enzyme gene IDE, has been identified as occur..." http://www.snpedia.com/index.php?title=Rs2209972 reference = Chr8 illumina rs2220456 84662096..84662096 "A study among Mongolians comparing ~800 tall (> 173cm) to ~800 short (<155cm) individuals concluded ..." http://www.snpedia.com/index.php?title=Rs2220456 reference = ChrX illumina rs2223841 66486896..66486896 "male-pattern baldness. Full text available. *G less likely to go bald before age 40 *A more likely t..." http://www.snpedia.com/index.php?title=Rs2223841 reference = Chr18 illumina rs222581 53468674..53468674 "" http://www.snpedia.com/index.php?title=Rs222581 reference = ChrX illumina rs2227098 122322643..122322643 "This SNP is part of a specific haplotype, rs989638-rs1034428-rs2227098 G-T-G (as oriented with respe..." http://www.snpedia.com/index.php?title=Rs2227098 reference = Chr13 both rs2227311 47885033..47885033 "This SNP has been linked to another SNP, rs4151620 which has been linked to ovarian cancer . More sp..." http://www.snpedia.com/index.php?title=Rs2227311 reference = Chr10 both rs2227564 75343107..75343107 "rs2227564 A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with..." http://www.snpedia.com/index.php?title=Rs2227564 reference = Chr1 both rs2227589 172152839..172152839 "[http://jama.ama-assn.org/cgi/content/short/299/11/1306 jama] deep vein thrombosis per risk allele o..." http://www.snpedia.com/index.php?title=Rs2227589 reference = Chr3 illumina rs2227928 143764302..143764302 "rs2227928, also known as Ex4+340C>T or T211M, is a SNP in the ATR gene. Although not significant on ..." http://www.snpedia.com/index.php?title=Rs2227928 reference = Chr17 illumina rs2227945 38497656..38497656 "This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs2227945 reference = Chr7 both rs2228006 5993301..5993301 "" http://www.snpedia.com/index.php?title=Rs2228006 reference = Chr5 snp rs2228043 55287688..55287688 "" http://www.snpedia.com/index.php?title=Rs2228043 reference = Chr8 both rs2228063 86580241..86580241 "[omim:CARBONIC ANHYDRASE II VARIANT]" http://www.snpedia.com/index.php?title=Rs2228063 reference = Chr4 snp rs2228119 178596954..178596954 "" http://www.snpedia.com/index.php?title=Rs2228119 reference = Chr16 illumina rs2228479 88513441..88513441 "rs2228479, known as Val92Met or V92M, is one of several SNPs in the MC1R gene commonly associated wi..." http://www.snpedia.com/index.php?title=Rs2228479 reference = Chr6 both rs2228480 152461788..152461788 "haplotype less common in schizophrenia rs2273206(T), rs2273207(G), rs2228480(G)." http://www.snpedia.com/index.php?title=Rs2228480 reference = Chr3 both rs2228561 48603018..48603018 "" http://www.snpedia.com/index.php?title=Rs2228561 reference = Chr3 illumina rs2228563 48599044..48599044 "" http://www.snpedia.com/index.php?title=Rs2228563 reference = Chr12 illumina rs2228576 6327323..6327323 "" http://www.snpedia.com/index.php?title=Rs2228576 reference = Chr7 snp rs2228595 86253923..86253923 "rs2228595 may contribute to risk for schizophrenia by modulating GRM3 splicing" http://www.snpedia.com/index.php?title=Rs2228595 reference = Chr19 illumina rs2228671 11071912..11071912 "15,000 individuals. Each copy of the minor T allele of SNP rs2228671 was related to a decrease of LD..." http://www.snpedia.com/index.php?title=Rs2228671 reference = Chr18 illumina rs2229080 48686600..48686600 "" http://www.snpedia.com/index.php?title=Rs2229080 reference = Chr6 illumina rs2229094 31648535..31648535 "Associated with at least one 'mortality outcome' in a study of ~10,000 individuals. 827 males and 70..." http://www.snpedia.com/index.php?title=Rs2229094 reference = Chr1 snp rs2229475 22054482..22054482 "" http://www.snpedia.com/index.php?title=Rs2229475 reference = Chr1 snp rs2229489 22041432..22041432 "" http://www.snpedia.com/index.php?title=Rs2229489 reference = Chr1 snp rs2229491 22041388..22041388 "" http://www.snpedia.com/index.php?title=Rs2229491 reference = Chr1 snp rs2229493 22032630..22032630 "" http://www.snpedia.com/index.php?title=Rs2229493 reference = Chr3 illumina rs2229519 81780820..81780820 "" http://www.snpedia.com/index.php?title=Rs2229519 reference = Chr2 illumina rs2229571 215353709..215353709 "" http://www.snpedia.com/index.php?title=Rs2229571 reference = Chr18 both rs2229616 56190256..56190256 "rs2229616, a variant in the MC4R gene known as V103I, has been associated with appetite regulation, ..." http://www.snpedia.com/index.php?title=Rs2229616 reference = Chr15 both rs2229765 97295748..97295748 "rs2229765(A;A) associated with ischemic stroke (OR = 1.641, P = 0.022) in a Chinese population" http://www.snpedia.com/index.php?title=Rs2229765 reference = Chr1 both rs2229857 152840591..152840591 "" http://www.snpedia.com/index.php?title=Rs2229857 reference = Chr4 snp rs2229940 46690123..46690123 "1050 nicotine-dependent cases and 879 non-dependent smoking controls rs279858 and rs16859834 aka rs2..." http://www.snpedia.com/index.php?title=Rs2229940 reference = Chr19 snp rs2230199 6669387..6669387 "rs2230199, a SNP in the complement component C3 gene, has been reported by several investigators to ..." http://www.snpedia.com/index.php?title=Rs2230199 reference = Chr19 snp rs2230201 6664291..6664291 "In ~500 Japanese SLE patients, the (G) allele of rs2230201, a SNP in the C3 gene, is associated with..." http://www.snpedia.com/index.php?title=Rs2230201 reference = Chr1 illumina rs2230288 153472791..153472791 "" http://www.snpedia.com/index.php?title=Rs2230288 reference = Chr1 illumina rs2230419 223673767..223673767 "" http://www.snpedia.com/index.php?title=Rs2230419 reference = Chr14 illumina rs2230500 60993992..60993992 "A common SNP only in Asian populations, this SNP (also known as 1425G/A) and a close neighbor also i..." http://www.snpedia.com/index.php?title=Rs2230500 reference = Chr9 illumina rs2230806 106660688..106660688 "[omim:CORONARY HEART DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA, PROTECTION AGAINST]" http://www.snpedia.com/index.php?title=Rs2230806 reference = Chr9 both rs2230808 106602625..106602625 "rs2297404, rs2230808, and rs2020927 haplotype (CAC) was more prevalent in the Alzheimer's disease gr..." http://www.snpedia.com/index.php?title=Rs2230808 reference = Chr12 both rs2230912 120106579..120106579 "rs2230912 has been reported to be associated with increased risk for bipolar disorder. The G allele..." http://www.snpedia.com/index.php?title=Rs2230912 reference = Chr6 illumina rs2230926 138237759..138237759 "An association was found between Systemic lupus erythematosus (SLE) and rs2230926." http://www.snpedia.com/index.php?title=Rs2230926 reference = ChrX illumina rs2234036 105166024..105166024 "[omim:THYROXINE-BINDING GLOBULIN, VARIANT A]" http://www.snpedia.com/index.php?title=Rs2234036 reference = Chr6 affy rs2234693 152205028..152205028 "rs2234693 is a SNP upstream of the estrogen alpha receptor ESR1 gene, and is sometimes referred to a..." http://www.snpedia.com/index.php?title=Rs2234693 reference = Chr1 illumina rs2234922 224093029..224093029 "[omim:EPOXIDE HYDROLASE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs2234922 reference = Chr7 illumina rs2235015 87037500..87037500 "rs2235015 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs2235015 reference = Chr7 both rs2235035 87017022..87017022 "C allele linked to colorectal cancers" http://www.snpedia.com/index.php?title=Rs2235035 reference = Chr7 both rs2235040 87003686..87003686 "rs2235040 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs2235040 reference = Chr7 illumina rs2235067 86987858..86987858 "rs2235067 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs2235067 reference = Chr1 both rs2235544 54148158..54148158 "rs2235544, was associated with the free T3 to free T4 ratio with genome-wide levels of significance ..." http://www.snpedia.com/index.php?title=Rs2235544 reference = Chr14 both rs2236225 63978598..63978598 "[omim:NEURAL TUBE DEFECTS, FOLATE-SENSITIVE, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs2236225 reference = Chr14 affy rs2236242 94029805..94029805 "rs2236242 with type-2 diabetes AA genotype bearing an increased risk (adjusted OR 2.35 [1.59; 3.46] ..." http://www.snpedia.com/index.php?title=Rs2236242 reference = Chr14 both rs2236316 50294167..50294167 "" http://www.snpedia.com/index.php?title=Rs2236316 reference = Chr1 snp rs2236851 25116141..25116141 "significant association between rs2236851 and ulcerative colitis (OR 1.61; 95% confidence interval [..." http://www.snpedia.com/index.php?title=Rs2236851 reference = Chr11 illumina rs2237892 2796327..2796327 "[http://spittoon.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-..." http://www.snpedia.com/index.php?title=Rs2237892 reference = Chr11 snp rs2237895 2813770..2813770 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.208.html nature] type-2 diabetes *rs2237895, ..." http://www.snpedia.com/index.php?title=Rs2237895 reference = Chr11 snp rs2237897 2815122..2815122 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.208.html nature] type-2 diabetes *rs2237897, ..." http://www.snpedia.com/index.php?title=Rs2237897 reference = Chr12 snp rs2238135 46564457..46564457 "rs2238135 is a SNP in the vitamin D VDR receptor gene. rs2238135(G;G) homozygotes were associated wi..." http://www.snpedia.com/index.php?title=Rs2238135 reference = Chr15 snp rs2238289 26126810..26126810 "rs2238289 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs2238289 reference = Chr16 illumina rs2238472 16159100..16159100 "[omim:PSEUDOXANTHOMA ELASTICUM]" http://www.snpedia.com/index.php?title=Rs2238472 reference = Chr6 illumina rs2239518 30973704..30973704 "schizophrenia the SNPs (rs1049623, rs2267641 and rs2239518) haplotype remaining significant even aft..." http://www.snpedia.com/index.php?title=Rs2239518 reference = Chr17 snp rs2240017 43165918..43165918 "This SNP encodes a variation in the 33rd amino acid of the protein encoded by the TBX21 gene. Althou..." http://www.snpedia.com/index.php?title=Rs2240017 reference = Chr15 illumina rs2240203 26167797..26167797 "rs2240203 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs2240203 reference = Chr17 illumina rs2240308 60985053..60985053 "" http://www.snpedia.com/index.php?title=Rs2240308 reference = Chr1 both rs2240335 17547124..17547124 "rs2240335 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumato..." http://www.snpedia.com/index.php?title=Rs2240335 reference = Chr1 snp rs2240338 17546772..17546772 "rs2240338 increases susceptibility to Rheumatoid Arthritis 1.82 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs2240338 reference = Chr1 snp rs2240339 17546695..17546695 "rs2240339 increases susceptibility to Rheumatoid Arthritis 1.75 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs2240339 reference = Chr1 snp rs2240340 17535226..17535226 "Several studies have all found that rs2240340, a SNP in the PADI4 gene, is associated with risk for ..." http://www.snpedia.com/index.php?title=Rs2240340 reference = Chr22 snp rs2240717 18349106..18349106 "" http://www.snpedia.com/index.php?title=Rs2240717 reference = Chr16 snp rs2241145 54079701..54079701 "association of the MMP-2 gene with the development of lacunar stroke. rs1030868, rs2241145, rs228707..." http://www.snpedia.com/index.php?title=Rs2241145 reference = Chr10 both rs224136 64140681..64140681 "rs224136 increases susceptibility to Crohn's disease 1.67 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs224136 reference = Chr19 snp rs2241524 59790479..59790479 "rs2241524 is a SNP in the LILRA2 gene that disrupts the splice acceptor site of intron 6. Case-contr..." http://www.snpedia.com/index.php?title=Rs2241524 reference = Chr19 snp rs2241712 46561596..46561596 "rs2241712, a SNP in the promoter region of the transforming growth factor beta1 TGFB1 gene has been ..." http://www.snpedia.com/index.php?title=Rs2241712 reference = Chr3 snp rs2241766 188053586..188053586 "A study of 733 breast cancer cases for 10 SNPs concluded that the rs2241766(G;T) genotype was at red..." http://www.snpedia.com/index.php?title=Rs2241766 reference = Chr8 illumina rs2241802 28440631..28440631 "[http://7thspace.com/headlines/290001/the_frizzled_3_gene_is_associated_with_methamphetamine_psychos..." http://www.snpedia.com/index.php?title=Rs2241802 reference = Chr2 illumina rs2241879 233848207..233848207 "rs2241879 has been associated with Crohn's disease; the minor allele is somewhat protective in that ..." http://www.snpedia.com/index.php?title=Rs2241879 reference = Chr2 illumina rs2241880 233848107..233848107 "rs2241880, a SNP in the ATG16L1 gene encoding a threonine to alanine substitution ('T300A') in a pro..." http://www.snpedia.com/index.php?title=Rs2241880 reference = Chr16 illumina rs224204 3236430..3236430 "rs224204 was associated with juvenile idiopathic arthritis based on a study of 950 Caucasian patient..." http://www.snpedia.com/index.php?title=Rs224204 reference = Chr6 illumina rs2242665 31947288..31947288 "" http://www.snpedia.com/index.php?title=Rs2242665 reference = Chr5 illumina rs2243250 132037053..132037053 "rs2243250 is a SNP in the IL4 gene that is also known as the -589C>T SNP. In 300 patients younger th..." http://www.snpedia.com/index.php?title=Rs2243250 reference = Chr6 illumina rs2243380 117831072..117831072 "" http://www.snpedia.com/index.php?title=Rs2243380 reference = Chr1 snp rs2245218 14012413..14012413 "rs2245218 increases susceptibility to Parkinson's disease 1.67 times for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs2245218 reference = Chr13 snp rs2249358 32521164..32521164 "rs2249358 is one of 2 SNPs (the other is rs211239) in the KLOTHO gene found in a study of ~150 sickl..." http://www.snpedia.com/index.php?title=Rs2249358 reference = Chr20 illumina rs2250889 44075813..44075813 "rs2250889, a SNP also known as P574R, is located in the MMP9 gene. In a study of 744 Chinese patient..." http://www.snpedia.com/index.php?title=Rs2250889 reference = Chr2 both rs2254958 37229795..37229795 "While the ApoE4 allele (rs429358(C)) is widely accepted as the predominant genetic risk factor for A..." http://www.snpedia.com/index.php?title=Rs2254958 reference = Chr3 snp rs2255543 121872006..121872006 "" http://www.snpedia.com/index.php?title=Rs2255543 reference = Chr5 illumina rs2255796 149731539..149731539 "rs2255796 and rs15251 suggested excess maternal transmission and may influence risk of cleft palate" http://www.snpedia.com/index.php?title=Rs2255796 reference = Chr17 both rs2258689 41423219..41423219 "" http://www.snpedia.com/index.php?title=Rs2258689 reference = Chr1 illumina rs2266782 169343590..169343590 "" http://www.snpedia.com/index.php?title=Rs2266782 reference = ChrX snp rs2266886 152884546..152884546 "rs2266886. The minor allele at this site displays an odds ratio of 0.26 (95% confidence intervals, 0..." http://www.snpedia.com/index.php?title=Rs2266886 reference = Chr22 snp rs2267012 21865982..21865982 "rs2267012, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs2267012 reference = Chr22 illumina rs2267013 21875879..21875879 "rs2267013, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs2267013 reference = Chr22 snp rs2267015 21888561..21888561 "rs2267015, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs2267015 reference = Chr6 snp rs2267641 30973183..30973183 "schizophrenia the SNPs (rs1049623, rs2267641 and rs2239518) haplotype remaining significant even aft..." http://www.snpedia.com/index.php?title=Rs2267641 reference = Chr6 illumina rs2267668 35485900..35485900 "rs1053049, rs6902123, and rs2267668 in PPARD affect Lifestyle Intervention induced changes in overal..." http://www.snpedia.com/index.php?title=Rs2267668 reference = ChrNone both rs2267801 2888196..2888196 "" http://www.snpedia.com/index.php?title=Rs2267801 reference = ChrNone illumina rs2267802 2888425..2888425 "" http://www.snpedia.com/index.php?title=Rs2267802 reference = Chr21 snp rs2268277 35103919..35103919 "rs7528684 rs3792876 and rs2268277 failed to showed a statistically significant association with rheu..." http://www.snpedia.com/index.php?title=Rs2268277 reference = ChrY illumina rs2268588 22919969..22919969 "" http://www.snpedia.com/index.php?title=Rs2268588 reference = ChrY snp rs2268591 22873985..22873985 "" http://www.snpedia.com/index.php?title=Rs2268591 reference = Chr22 illumina rs2269529 35014300..35014300 "" http://www.snpedia.com/index.php?title=Rs2269529 reference = Chr1 snp rs2269648 167822674..167822674 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0030120...." http://www.snpedia.com/index.php?title=Rs2269648 reference = Chr12 snp rs2270031 1612770..1612770 "IVS3C>G variant (rs2270031) may influence type-2 diabetes" http://www.snpedia.com/index.php?title=Rs2270031 reference = Chr8 affy rs2270641 20082746..20082746 "rs2270641 is a SNP in the vesicular monoamine transporter SLC18A1 gene, encoding a Thr4Pro substitut..." http://www.snpedia.com/index.php?title=Rs2270641 reference = Chr2 snp rs2270669 237908203..237908203 "" http://www.snpedia.com/index.php?title=Rs2270669 reference = Chr3 illumina rs2270968 184237903..184237903 "" http://www.snpedia.com/index.php?title=Rs2270968 reference = Chr2 snp rs2272127 102406305..102406305 "associations with schizophrenia and herpes rs2272127 with schizophrenia(P = 0.0007, odds ratio for C..." http://www.snpedia.com/index.php?title=Rs2272127 reference = Chr7 snp rs2272263 55401378..55401378 "" http://www.snpedia.com/index.php?title=Rs2272263 reference = Chr11 snp rs2272382 8068116..8068116 "rs2272382, a SNP in the TUB gene, was found in a study of 492 unrelated type-2 diabetes patients to ..." http://www.snpedia.com/index.php?title=Rs2272382 reference = Chr11 snp rs2272383 8080075..8080075 "rs2272383, a SNP in the TUB gene, was found in a study of 492 unrelated type-2 diabetes patients to ..." http://www.snpedia.com/index.php?title=Rs2272383 reference = Chr12 both rs2272495 104108007..104108007 "" http://www.snpedia.com/index.php?title=Rs2272495 reference = Chr6 both rs2273206 152424004..152424004 "haplotype less common in schizophrenia rs2273206(T), rs2273207(G), rs2228480(G)." http://www.snpedia.com/index.php?title=Rs2273206 reference = Chr6 affy rs2273207 152424018..152424018 "haplotype less common in schizophrenia rs2273206(T), rs2273207(G), rs2228480(G)." http://www.snpedia.com/index.php?title=Rs2273207 reference = Chr20 snp rs2273535 54394948..54394948 "SNP rs2273535, also known as F31I or Phe31Ile, has been associated with increased risk for several c..." http://www.snpedia.com/index.php?title=Rs2273535 reference = Chr4 illumina rs227368 103830893..103830893 "" http://www.snpedia.com/index.php?title=Rs227368 reference = Chr9 illumina rs2274158 116206027..116206027 "" http://www.snpedia.com/index.php?title=Rs2274158 reference = Chr9 illumina rs2274159 116206067..116206067 "" http://www.snpedia.com/index.php?title=Rs2274159 reference = Chr1 snp rs2275166 16252830..16252830 "" http://www.snpedia.com/index.php?title=Rs2275166 reference = Chr1 snp rs2275351 201416696..201416696 "schizophrenia *375 case and 812 control subjects *rs10399805 p = .018 and rs2275351; p = .008." http://www.snpedia.com/index.php?title=Rs2275351 reference = Chr11 snp rs2276288 76590284..76590284 "" http://www.snpedia.com/index.php?title=Rs2276288 reference = Chr15 illumina rs2277598 70814531..70814531 "" http://www.snpedia.com/index.php?title=Rs2277598 reference = Chr5 both rs2278008 34025275..34025275 "" http://www.snpedia.com/index.php?title=Rs2278008 reference = Chr2 illumina rs2278206 98538676..98538676 "A study of ~170 families led to a slight association between rs2278206 and atopic asthma. The risk g..." http://www.snpedia.com/index.php?title=Rs2278206 reference = Chr10 illumina rs2279420 61451953..61451953 "Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio..." http://www.snpedia.com/index.php?title=Rs2279420 reference = Chr12 snp rs2279744 67488847..67488847 "rs2279744, a variant in the promoter of the MDM2 also known as '-410T-G' and 'SNP309', has been stud..." http://www.snpedia.com/index.php?title=Rs2279744 reference = Chr20 illumina rs2280089 3598127..3598127 "rs2280089, a SNP in the ADAM33 gene, has been linked to a predisposition to asthma and bronchial hyp..." http://www.snpedia.com/index.php?title=Rs2280089 reference = Chr20 snp rs2280090 3598205..3598205 "rs2280090, a SNP in the ADAM33 gene, has been linked to a predisposition to asthma and bronchial hyp..." http://www.snpedia.com/index.php?title=Rs2280090 reference = Chr7 illumina rs2280714 128381961..128381961 "The rs2004640 T allele had a higher frequency in SLE cases (0.385) than controls (0.321; odds ratio ..." http://www.snpedia.com/index.php?title=Rs2280714 reference = Chr8 illumina rs2280838 145612810..145612810 "" http://www.snpedia.com/index.php?title=Rs2280838 reference = Chr1 illumina rs2281845 199348566..199348566 "[omim:THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs2281845 reference = Chr9 snp rs2281999 35371504..35371504 "rs2281999 and rs13293564 (G/T) diabetic nephropathy type-1 diabetes case/control (1176/1323) study f..." http://www.snpedia.com/index.php?title=Rs2281999 reference = Chr11 affy rs2283228 2806106..2806106 "[http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.208.html nature] type-2 diabetes *rs2283228 (..." http://www.snpedia.com/index.php?title=Rs2283228 reference = ChrX both rs228406 32413115..32413115 "" http://www.snpedia.com/index.php?title=Rs228406 reference = Chr17 illumina rs2285644 39684147..39684147 "[omim:DIEGO BLOOD GROUP ANTIGEN]" http://www.snpedia.com/index.php?title=Rs2285644 reference = Chr11 both rs228591 107602543..107602543 "rs8178085 and rs12334811 with approaching dose-dependent effect on lung cancer predisposition, subje..." http://www.snpedia.com/index.php?title=Rs228591 reference = Chr19 illumina rs2286662 17793138..17793138 "" http://www.snpedia.com/index.php?title=Rs2286662 reference = Chr3 illumina rs2286983 173775178..173775178 "SNP rs2286983 has been associated with both cholesterol levels and body-mass index (eg obesity) in t..." http://www.snpedia.com/index.php?title=Rs2286983 reference = Chr16 snp rs2287074 54084614..54084614 "association of the MMP-2 gene with the development of lacunar stroke. rs1030868, rs2241145, rs228707..." http://www.snpedia.com/index.php?title=Rs2287074 reference = Chr16 illumina rs2287076 54089959..54089959 "association of the MMP-2 gene with the development of lacunar stroke. rs1030868, rs2241145, rs228707..." http://www.snpedia.com/index.php?title=Rs2287076 reference = Chr17 illumina rs2287499 7532893..7532893 "ER negative breast cancer association rs2287499, OR (95% CI) = 1.08 (0.95-1.23) for CG vs. CC and 1...." http://www.snpedia.com/index.php?title=Rs2287499 reference = Chr2 illumina rs2287622 169538574..169538574 "" http://www.snpedia.com/index.php?title=Rs2287622 reference = Chr5 illumina rs2287939 34034640..34034640 "" http://www.snpedia.com/index.php?title=Rs2287939 reference = Chr5 illumina rs2287987 96155291..96155291 "rs2287987 is one of several SNPs in the ARTS1 gene that has been shown in a large (over 1,000 Caucas..." http://www.snpedia.com/index.php?title=Rs2287987 reference = Chr16 illumina rs2288033 77803462..77803462 "" http://www.snpedia.com/index.php?title=Rs2288033 reference = Chr16 snp rs2288034 77803457..77803457 "" http://www.snpedia.com/index.php?title=Rs2288034 reference = Chr18 illumina rs2288774 54134310..54134310 "rs2288774 has been associated with hypertension. In genotypic combination with rs4149601 it was asso..." http://www.snpedia.com/index.php?title=Rs2288774 reference = Chr19 both rs2288904 10603170..10603170 "" http://www.snpedia.com/index.php?title=Rs2288904 reference = Chr16 snp rs2289116 55495791..55495791 "Associated with diabetic nephropathy and type-2 diabetes in a Japanese population." http://www.snpedia.com/index.php?title=Rs2289116 reference = Chr4 snp rs2290602 23434830..23434830 "rs2290602 is a SNP in the PPARGC1A gene that has been associated with nonalcoholic fatty liver disea..." http://www.snpedia.com/index.php?title=Rs2290602 reference = Chr5 snp rs2291418 179157930..179157930 "" http://www.snpedia.com/index.php?title=Rs2291418 reference = Chr7 snp rs2291569 128275970..128275970 "" http://www.snpedia.com/index.php?title=Rs2291569 reference = Chr12 both rs2292239 54768447..54768447 "In an expanded follow-up study of >6,000 controls and 6,000 patients, in which rs2292239 was chosen ..." http://www.snpedia.com/index.php?title=Rs2292239 reference = Chr16 illumina rs2292954 88140624..88140624 "" http://www.snpedia.com/index.php?title=Rs2292954 reference = Chr2 both rs2293275 48774879..48774879 "SNP in the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) gene, correlated to spermatog..." http://www.snpedia.com/index.php?title=Rs2293275 reference = Chr7 illumina rs2293507 69865956..69865956 "" http://www.snpedia.com/index.php?title=Rs2293507 reference = Chr8 snp rs2293869 55701948..55701948 "[omim:HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs2293869 reference = Chr10 snp rs2293870 124211266..124211266 "rs2293870 showed as strong an association with increased susceptibility to neovascular age related m..." http://www.snpedia.com/index.php?title=Rs2293870 reference = Chr8 illumina rs2294008 143758933..143758933 "rs2976392 and diffuse-type gastric cancer (allele-specific odds ratio (OR) = 1.62, 95% CI = 1.38-1.8..." http://www.snpedia.com/index.php?title=Rs2294008 reference = Chr6 snp rs2296336 33744638..33744638 "rs2296336 has been reported in a Swedish study to be associated with type-1 diabetes. The risk allel..." http://www.snpedia.com/index.php?title=Rs2296336 reference = Chr9 illumina rs2296949 133375257..133375257 "" http://www.snpedia.com/index.php?title=Rs2296949 reference = Chr9 snp rs2297404 106604287..106604287 "rs2297404, rs2230808, and rs2020927 haplotype (CAC) was more prevalent in the Alzheimer's disease gr..." http://www.snpedia.com/index.php?title=Rs2297404 reference = Chr1 illumina rs2297480 153546106..153546106 "rs2297480 is a SNP in the FDPS gene, which encodes an enzyme in the mevalonate pathway and therefore..." http://www.snpedia.com/index.php?title=Rs2297480 reference = Chr17 snp rs2297508 17656042..17656042 "rs2297508 is one of several SNPs associated with the SREBF1 gene that show a modest association with..." http://www.snpedia.com/index.php?title=Rs2297508 reference = Chr1 illumina rs2297950 201460809..201460809 "" http://www.snpedia.com/index.php?title=Rs2297950 reference = Chr11 illumina rs2298566 130255852..130255852 "rs2298566 is a SNP in the MYH15 gene. The risk allele in terms of heart disease is rs2298566(C). Thi..." http://www.snpedia.com/index.php?title=Rs2298566 reference = Chr11 snp rs2298668 82241942..82241942 "Women with the snp has been linked to significant risk of a premature birth These [http://www.eurek..." http://www.snpedia.com/index.php?title=Rs2298668 reference = Chr7 both rs2300045 107850474..107850474 "Based on a study of 170 patients with autism, this SNP (rs2300045) in the NRCAM gene and a haplotype..." http://www.snpedia.com/index.php?title=Rs2300045 reference = Chr21 snp rs2300403 46845482..46845482 "associated Alzheimer's disease especially in women, increasing the risk of low cognitive performance..." http://www.snpedia.com/index.php?title=Rs2300403 reference = Chr2 both rs2300478 66634957..66634957 "rs2300478, a SNP located in the MEIS1 gene, has been linked to restless legs syndrome, a common slee..." http://www.snpedia.com/index.php?title=Rs2300478 reference = Chr9 snp rs2300929 122756661..122756661 "[omim:LIVER FIBROSIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs2300929 reference = Chr9 snp rs2301612 135291803..135291803 "[omim:THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs2301612 reference = Chr1 illumina rs2301888 17545317..17545317 "rs2301888 increases susceptibility to Rheumatoid Arthritis 1.82 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs2301888 reference = Chr7 illumina rs2302009 75236934..75236934 "rs2302009 is a SNP located in the 3' untranslated region of the CCL26 gene. This gene (and this SNP)..." http://www.snpedia.com/index.php?title=Rs2302009 reference = Chr4 illumina rs2302075 5806443..5806443 "" http://www.snpedia.com/index.php?title=Rs2302075 reference = Chr17 illumina rs2302254 46585899..46585899 "breast cancer 1,134 breast cancer patients recruited as part of the Shanghai Breast Cancer Study who..." http://www.snpedia.com/index.php?title=Rs2302254 reference = Chr12 illumina rs2302685 12193165..12193165 "rs2302685 increases susceptibility to Alzheimer's disease, late-onset 1.30 times for carriers of the..." http://www.snpedia.com/index.php?title=Rs2302685 reference = Chr17 both rs2302762 7299585..7299585 "Variations in this snp have been linked to nicotine dependence" http://www.snpedia.com/index.php?title=Rs2302762 reference = Chr17 snp rs2302763 7300001..7300001 "Variations in this snp have been linked to nicotine dependence" http://www.snpedia.com/index.php?title=Rs2302763 reference = Chr17 illumina rs2302765 7291699..7291699 "Variations in this snp have been linked to nicotine dependence [http://www.ncbi.nlm.nih.gov/entrez/q..." http://www.snpedia.com/index.php?title=Rs2302765 reference = Chr5 illumina rs2303063 147460220..147460220 "" http://www.snpedia.com/index.php?title=Rs2303063 reference = Chr5 both rs2303064 147460273..147460273 "rs2303064, a SNP in the SPINK5 gene, has been associated with susceptibility to atopic dermatitis." http://www.snpedia.com/index.php?title=Rs2303064 reference = Chr5 illumina rs2303067 147461148..147461148 "rs2303067, a SNP in the SPINK5 gene, has been significantly associated with susceptibility to atopic..." http://www.snpedia.com/index.php?title=Rs2303067 reference = Chr11 both rs2303436 111401534..111401534 "" http://www.snpedia.com/index.php?title=Rs2303436 reference = Chr16 both rs2303790 55574793..55574793 "[omim:CHOLESTEROL ESTER TRANSFER PROTEIN DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs2303790 reference = Chr19 both rs2304256 10336652..10336652 "rs2304256 is a SNP in the TYK2 gene on chromosome 19. The most common allele, rs2304256(C), has been..." http://www.snpedia.com/index.php?title=Rs2304256 reference = Chr2 illumina rs2305560 198074033..198074033 "G-C-T-C haplotype of rs2340690-rs788016-rs2305560-rs2565163 has odds ratio of 1.91 (CI: 1.26-2.89, p..." http://www.snpedia.com/index.php?title=Rs2305560 reference = Chr19 illumina rs2305764 17174833..17174833 "rs2305764 is a SNP in the untranslated region of the MYO9B gene that has been associated with celiac..." http://www.snpedia.com/index.php?title=Rs2305764 reference = Chr19 illumina rs2305767 17155296..17155296 "rs2305767 (P = 1.16 x 10(-4); OR 1.41, 95% CI 1.18-1.67). We demonstrate significant association of ..." http://www.snpedia.com/index.php?title=Rs2305767 reference = Chr11 illumina rs2306033 46854022..46854022 "rs2306033 increases susceptibility to Osteoporotic fractures for carriers of the G allele" http://www.snpedia.com/index.php?title=Rs2306033 reference = Chr12 illumina rs2306180 21604669..21604669 "" http://www.snpedia.com/index.php?title=Rs2306180 reference = Chr12 illumina rs2306283 21221005..21221005 "[http://www.genomeweb.com/issues/news/148953-1.html?CMP=OTC-RSS news] rs2306283 influences statin-re..." http://www.snpedia.com/index.php?title=Rs2306283 reference = Chr10 illumina rs2306402 68605491..68605491 "Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio..." http://www.snpedia.com/index.php?title=Rs2306402 reference = Chr12 illumina rs2306536 131933735..131933735 "rs2306536, a SNP in the CHFR gene, was found to be significantly associated with a lower risk of col..." http://www.snpedia.com/index.php?title=Rs2306536 reference = Chr12 illumina rs2306541 131938315..131938315 "" http://www.snpedia.com/index.php?title=Rs2306541 reference = Chr4 snp rs2306985 100735045..100735045 "" http://www.snpedia.com/index.php?title=Rs2306985 reference = Chr4 snp rs2306986 100723598..100723598 "" http://www.snpedia.com/index.php?title=Rs2306986 reference = Chr10 illumina rs2308321 131455054..131455054 "rs2308321, also known as Ile143Val or I143V, is a SNP in the MGMT gene. The more common (A) allele e..." http://www.snpedia.com/index.php?title=Rs2308321 reference = Chr10 illumina rs2308327 131455160..131455160 "rs2308327, also known as K178R, is a SNP in the MGMT gene. The more common allele, rs2308327(A), enc..." http://www.snpedia.com/index.php?title=Rs2308327 reference = Chr9 both rs2309428 71032843..71032843 "" http://www.snpedia.com/index.php?title=Rs2309428 reference = Chr4 both rs2313982 139007510..139007510 "rs2313982 increases susceptibility to Parkinson's disease 2.01 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs2313982 reference = Chr19 snp rs231591 40916545..40916545 "" http://www.snpedia.com/index.php?title=Rs231591 reference = Chr2 illumina rs231775 204440959..204440959 "rs231775 (CTLA4_+49_G/A P=0.0219) and rs733618 (CTLA4_-1722_T/C P=0.0096) susceptibility to Graves' ..." http://www.snpedia.com/index.php?title=Rs231775 reference = ChrNone snp rs2319818 14864102..14864102 "" http://www.snpedia.com/index.php?title=Rs2319818 reference = Chr2 both rs2322659 136272129..136272129 "" http://www.snpedia.com/index.php?title=Rs2322659 reference = Chr8 snp rs2323019 28446889..28446889 "[http://7thspace.com/headlines/290001/the_frizzled_3_gene_is_associated_with_methamphetamine_psychos..." http://www.snpedia.com/index.php?title=Rs2323019 reference = Chr22 affy rs2331291 25388821..25388821 "rs2331291 a non-coding RNA, MIAT, that confers risk of Myocardial infarction." http://www.snpedia.com/index.php?title=Rs2331291 reference = Chr17 snp rs2333227 53713761..53713761 "rs2333227 is a SNP in the promoter region of the myeloperoxidase MPO gene; it is also known as the -..." http://www.snpedia.com/index.php?title=Rs2333227 reference = Chr2 illumina rs2340690 198069131..198069131 "G-C-T-C haplotype of rs2340690-rs788016-rs2305560-rs2565163 has odds ratio of 1.91 (CI: 1.26-2.89, p..." http://www.snpedia.com/index.php?title=Rs2340690 reference = Chr21 illumina rs235326 45136241..45136241 "651 people of Japanese ethnicity, of which 274 were Japanese Americans living in Hawaii, and the rem..." http://www.snpedia.com/index.php?title=Rs235326 reference = Chr21 snp rs235330 45139335..45139335 "" http://www.snpedia.com/index.php?title=Rs235330 reference = Chr20 snp rs235754 6715677..6715677 "SNP rs235754, a variant located in the 3' region of the bone morphogenic protein-2 BMP2, has been re..." http://www.snpedia.com/index.php?title=Rs235754 reference = Chr20 illumina rs235756 6715111..6715111 "rs235756, a relatively common SNP in the BMP2 gene, has been associated with higher serum transferri..." http://www.snpedia.com/index.php?title=Rs235756 reference = Chr10 snp rs2368392 29874009..29874009 "" http://www.snpedia.com/index.php?title=Rs2368392 reference = Chr6 affy rs237025 149763383..149763383 "suggests the contribution of rs237025 to both type-1 diabetes|type 1 and type-2 diabetes|type 2 diab..." http://www.snpedia.com/index.php?title=Rs237025 reference = Chr5 affy rs2371685 40427983..40427983 "rs2371685 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's ..." http://www.snpedia.com/index.php?title=Rs2371685 reference = Chr2 snp rs2372536 215898265..215898265 "" http://www.snpedia.com/index.php?title=Rs2372536 reference = Chr11 affy rs2373115 77768798..77768798 "rs2373115 is one of several SNPs in the GAB2 gene indicating an increased risk (OR 4.1) of late-onse..." http://www.snpedia.com/index.php?title=Rs2373115 reference = Chr17 both rs238238 4797122..4797122 "" http://www.snpedia.com/index.php?title=Rs238238 reference = Chr9 snp rs2383206 22105026..22105026 "rs10757274 and rs2383206 can double the risk of heart disease[http://www.sciencemag.org/cgi/content/..." http://www.snpedia.com/index.php?title=Rs2383206 reference = Chr9 illumina rs2383207 22105959..22105959 "discussed in this [http://suicyte.wordpress.com/2007/05/26/soul-searching-i/ blog post] as possibly ..." http://www.snpedia.com/index.php?title=Rs2383207 reference = Chr6 illumina rs2395029 31539759..31539759 "This SNP is thought to be involved in determining the HIV viral load set point during the asymptomat..." http://www.snpedia.com/index.php?title=Rs2395029 reference = Chr15 both rs2398162 94631554..94631554 "rs2398162 has been reported in a large study to be associated with high blood pressure. The risk all..." http://www.snpedia.com/index.php?title=Rs2398162 reference = ChrX snp rs2407992 12849033..12849033 "A study of ~900 Danish subjects concluded that rs2407992 showed the most significant association wit..." http://www.snpedia.com/index.php?title=Rs2407992 reference = Chr4 both rs2412522 54633300..54633300 "risk of cardiovascular disease rs2412522 for mean corpuscular hemoglobin concentration was 7*10(-8)" http://www.snpedia.com/index.php?title=Rs2412522 reference = Chr15 illumina rs2412541 38701132..38701132 "" http://www.snpedia.com/index.php?title=Rs2412541 reference = Chr22 snp rs2413338 33993523..33993523 "psychotic bipolar affective disorder. Genotype-wise analyses yielded similar results, but the psycho..." http://www.snpedia.com/index.php?title=Rs2413338 reference = Chr6 illumina rs241447 32904728..32904728 "[omim:PEPTIDE TRANSPORTER PSF2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs241447 reference = Chr6 illumina rs241448 32904662..32904662 "While the ApoE4 allele (rs429358(C)) is widely accepted as the predominant genetic risk factor for A..." http://www.snpedia.com/index.php?title=Rs241448 reference = Chr9 affy rs2416804 122716217..122716217 "rs2416804 increases susceptibility to Rheumatoid Arthritis 1.25 times for heterozygotes (CG) and 1.6..." http://www.snpedia.com/index.php?title=Rs2416804 reference = Chr9 snp rs2416806 122730113..122730113 "rs2416806 increases susceptibility to Rheumatoid Arthritis 1.36 times for heterozygotes (CG) and 1.5..." http://www.snpedia.com/index.php?title=Rs2416806 reference = Chr9 snp rs2416808 122746104..122746104 "* See rs10818488" http://www.snpedia.com/index.php?title=Rs2416808 reference = Chr10 illumina rs2420946 123341314..123341314 "This SNP is basically a proxy for SNP rs1219648, which represents the SNP in the FGFR2 gene with the..." http://www.snpedia.com/index.php?title=Rs2420946 reference = Chr6 both rs2435322 51983209..51983209 "" http://www.snpedia.com/index.php?title=Rs2435322 reference = Chr10 snp rs2435357 42902062..42902062 "This SNP, located in the first intron of the RET gene, has been associated with Hirschsprung disease..." http://www.snpedia.com/index.php?title=Rs2435357 reference = Chr2 both rs2437896 176030735..176030735 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs2437896 reference = Chr8 affy rs2442496 6314682..6314682 "rs964201 and rs2442496 arose approximately 50,000 years ago and show strong positive selection in th..." http://www.snpedia.com/index.php?title=Rs2442496 reference = Chr8 illumina rs2442513 6283958..6283958 "" http://www.snpedia.com/index.php?title=Rs2442513 reference = Chr4 both rs2452600 95715905..95715905 "" http://www.snpedia.com/index.php?title=Rs2452600 reference = Chr12 illumina rs2464196 119919810..119919810 "" http://www.snpedia.com/index.php?title=Rs2464196 reference = Chr1 illumina rs2476601 114179091..114179091 "This SNP, located in the PTPN22 gene and also known as R620W, or 1858C>T, may influence Rheumatoid A..." http://www.snpedia.com/index.php?title=Rs2476601 reference = Chr6 snp rs2479717 42013152..42013152 "associated with prognosis after a diagnosis of breast cancer" http://www.snpedia.com/index.php?title=Rs2479717 reference = Chr1 snp rs2482965 156886352..156886352 "" http://www.snpedia.com/index.php?title=Rs2482965 reference = Chr9 snp rs2488601 125175536..125175536 "" http://www.snpedia.com/index.php?title=Rs2488601 reference = Chr9 both rs2491097 102042272..102042272 "" http://www.snpedia.com/index.php?title=Rs2491097 reference = Chr9 illumina rs2491397 100244983..100244983 "Associated with nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs2491397 reference = Chr1 snp rs2494876 50439102..50439102 "" http://www.snpedia.com/index.php?title=Rs2494876 reference = Chr1 affy rs2499846 160199672..160199672 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs2499846 reference = Chr10 illumina rs2505535 42913049..42913049 "the C allele of rs2505535 would appear to represent a protecting allele for the Chinese population" http://www.snpedia.com/index.php?title=Rs2505535 reference = Chr5 illumina rs251124 82841180..82841180 "failed to reproduce evidence of intracranial aneurysms in a Han Chinese population [http://stroke.ah..." http://www.snpedia.com/index.php?title=Rs251124 reference = Chr5 both rs251177 141007068..141007068 "rs251177 is one of seven SNPs found in a combined study of over 1,000 patients to be associated with..." http://www.snpedia.com/index.php?title=Rs251177 reference = Chr8 illumina rs2515569 6289826..6289826 "" http://www.snpedia.com/index.php?title=Rs2515569 reference = Chr1 affy rs2516839 159279745..159279745 "carriers of risk alleles of rs2516839 also showed a 2-fold risk for sudden cardiac death (genotype T..." http://www.snpedia.com/index.php?title=Rs2516839 reference = Chr3 illumina rs2518136 187820521..187820521 "Associated with type-2 diabetes in a study of Danish (but apparently not Swedish or French) Caucasia..." http://www.snpedia.com/index.php?title=Rs2518136 reference = Chr6 illumina rs2518224 102013370..102013370 "This SNP, located in an intron of the GRIK2 gene, has been linked in one study to increased thoughts..." http://www.snpedia.com/index.php?title=Rs2518224 reference = Chr7 snp rs2522943 73452685..73452685 "" http://www.snpedia.com/index.php?title=Rs2522943 reference = ChrNone illumina rs2534636 2717176..2717176 "" http://www.snpedia.com/index.php?title=Rs2534636 reference = Chr7 snp rs2538991 147210552..147210552 "Reported to be in very tight (r2>0.98) linkage with rs2710102, and thus potentially assoc..." http://www.snpedia.com/index.php?title=Rs2538991 reference = Chr18 both rs2542151 12769947..12769947 "rs2542151 has been reported in a large study to be associated with Crohn's disease. The risk allele ..." http://www.snpedia.com/index.php?title=Rs2542151 reference = Chr5 affy rs2544677 86435018..86435018 "rs2544677 has been reported in a large study to be associated with type-1 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs2544677 reference = Chr19 illumina rs25487 48747566..48747566 "rs25487 is a SNP also known as Gln399Arg, located in the DNA repair gene XRCC1. The (A) allele encod..." http://www.snpedia.com/index.php?title=Rs25487 reference = Chr16 illumina rs2548861 77215894..77215894 "9,798 subjects show significant association between rs2548861(T) and Low serum HDL-cholesterol, a ma..." http://www.snpedia.com/index.php?title=Rs2548861 reference = Chr19 illumina rs25489 48748252..48748252 "rs25489, a SNP also known as Arg280His located in the DNA-repair gene XRCC1, is associated with an i..." http://www.snpedia.com/index.php?title=Rs25489 reference = Chr17 snp rs25531 25588472..25588472 "In contrast to earlier reports linking rs25531, a SNP in the serotonin transporter SLC6A4 gene, to o..." http://www.snpedia.com/index.php?title=Rs25531 reference = Chr8 snp rs2553268 31055898..31055898 "exercise systolic blood pressure, rs2553268 (WRN, p = 6.3*10(-6));" http://www.snpedia.com/index.php?title=Rs2553268 reference = Chr15 both rs25651 88136792..88136792 "" http://www.snpedia.com/index.php?title=Rs25651 reference = Chr2 illumina rs2565163 198062659..198062659 "G-C-T-C haplotype of rs2340690-rs788016-rs2305560-rs2565163 has odds ratio of 1.91 (CI: 1.26-2.89, p..." http://www.snpedia.com/index.php?title=Rs2565163 reference = Chr5 snp rs2569190 139993100..139993100 "stroke rs2569190(C) (frequency = 39%) increase risk among smokers (OR = 2.05, 95% CI=1.09-3.86, p=0...." http://www.snpedia.com/index.php?title=Rs2569190 reference = Chr19 snp rs2569788 10375159..10375159 "" http://www.snpedia.com/index.php?title=Rs2569788 reference = Chr8 both rs2572886 143900157..143900157 "rs2572886 is a SNP determined by both linkage studies and in-vitro experiments to increase the susce..." http://www.snpedia.com/index.php?title=Rs2572886 reference = Chr3 illumina rs2593813 187815265..187815265 "Category:is a snp [http://cat.inist.fr/?aModele=afficheN&cpsidt=16815755] Homozygosity for the rs259..." http://www.snpedia.com/index.php?title=Rs2593813 reference = Chr2 affy rs2600683 175338721..175338721 "rs2600683 increases susceptibility to Myasthenia gravis, early onset 2.36 times for carriers of the ..." http://www.snpedia.com/index.php?title=Rs2600683 reference = Chr2 snp rs260630 108893805..108893805 "" http://www.snpedia.com/index.php?title=Rs260630 reference = Chr15 snp rs2606345 72804229..72804229 "577 testicular germ cell tumors cases (254 seminoma, 323 nonseminoma) and 707 controls. inversely as..." http://www.snpedia.com/index.php?title=Rs2606345 reference = Chr8 affy rs2609653 34356534..34356534 "rs2609653 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs2609653 reference = Chr15 both rs261332 56514617..56514617 "rs261332 increases susceptibility to Elevated HDL-Cholesterol for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs261332 reference = Chr12 affy rs2617160 10436864..10436864 "This SNP is part of a haplotype reported for the KLRK1 gene, potentially associated with risk for co..." http://www.snpedia.com/index.php?title=Rs2617160 reference = Chr12 both rs2617170 10452224..10452224 "This SNP is part of a haplotype reported for the KLRK1 gene, potentially associated with risk for co..." http://www.snpedia.com/index.php?title=Rs2617170 reference = Chr12 snp rs2617171 10452546..10452546 "This SNP is part of a haplotype reported for the KLRK1 gene, potentially associated with risk for co..." http://www.snpedia.com/index.php?title=Rs2617171 reference = Chr17 both rs2619112 4482134..4482134 "rs2619112 and rs916055 are associated with high bone mineral density in pre-menopausal women but low..." http://www.snpedia.com/index.php?title=Rs2619112 reference = Chr6 illumina rs2619522 15761628..15761628 "[http://originsgenomeresources.net/musings/?p=85 blog] In a population of healthy individuals, those..." http://www.snpedia.com/index.php?title=Rs2619522 reference = Chr12 affy rs2630578 32197054..32197054 "People with the C version of rs2630578(C) have telomeres in their white blood cells that are between..." http://www.snpedia.com/index.php?title=Rs2630578 reference = Chr12 snp rs2630778 37336856..37336856 "Influences telomere length, which is relevant to aging. Subjects carrying the C allele for rs2630778..." http://www.snpedia.com/index.php?title=Rs2630778 reference = Chr5 snp rs2631367 131733357..131733357 "rs2631367, a SNP in the promoter region of the SLC22A5 gene, has been associated with an autoimmune ..." http://www.snpedia.com/index.php?title=Rs2631367 reference = Chr5 affy rs2631372 131731477..131731477 "rs2631372 increases susceptibility to Crohn's disease 1.28 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs2631372 reference = Chr4 illumina rs2637777 187762014..187762014 "associated with bipolar disorder" http://www.snpedia.com/index.php?title=Rs2637777 reference = Chr12 illumina rs2638525 51493895..51493895 "" http://www.snpedia.com/index.php?title=Rs2638525 reference = Chr1 both rs2639703 223879534..223879534 "rs2639703 has been reported in a large study to be associated with type-1 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs2639703 reference = Chr17 both rs2643103 56141407..56141407 "" http://www.snpedia.com/index.php?title=Rs2643103 reference = Chr6 both rs2653349 55250296..55250296 "rs2653349, also known as G1246A, is a SNP in the HCRTR2 hypocretin-orexin gene. It has been linked p..." http://www.snpedia.com/index.php?title=Rs2653349 reference = Chr5 illumina rs265981 174803508..174803508 "Implicated as part of a haplotype of the dopamine D1 receptor DRD1 gene associated with autism spect..." http://www.snpedia.com/index.php?title=Rs265981 reference = Chr3 illumina rs2660753 87193364..87193364 "[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-g..." http://www.snpedia.com/index.php?title=Rs2660753 reference = Chr12 illumina rs2660899 94954551..94954551 "Despite earlier reports of an association, no risk for myocardial infarction was seen for rs2660899 ..." http://www.snpedia.com/index.php?title=Rs2660899 reference = Chr3 snp rs266714 187981619..187981619 "maybe connected to type-2 diabetes?" http://www.snpedia.com/index.php?title=Rs266714 reference = Chr17 snp rs2670660 5459730..5459730 "linked to generalized vitiligo Individuals carrying high-risk alleles of both rs6502867 and rs26706..." http://www.snpedia.com/index.php?title=Rs2670660 reference = Chr5 illumina rs26722 33999627..33999627 "Although the rs26722(T) alllele is relatively rare, at least statistically it seems to be associated..." http://www.snpedia.com/index.php?title=Rs26722 reference = Chr10 snp rs2672598 124210672..124210672 "*rs11200638 1.7x10-14 (-625G>A)is the most significant associated SNP with a high OR of 7.6 (95%CI: ..." http://www.snpedia.com/index.php?title=Rs2672598 reference = Chr15 affy rs2679117 63276741..63276741 "" http://www.snpedia.com/index.php?title=Rs2679117 reference = Chr15 both rs2679118 63277954..63277954 "" http://www.snpedia.com/index.php?title=Rs2679118 reference = Chr8 illumina rs268 19857809..19857809 "rs268, a SNP in the lipoprotein lipase LPL gene, has been linked to increased susceptibility to idio..." http://www.snpedia.com/index.php?title=Rs268 reference = Chr3 illumina rs2692696 134967823..134967823 "" http://www.snpedia.com/index.php?title=Rs2692696 reference = Chr1 both rs2697962 14023579..14023579 "rs2697962 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinso..." http://www.snpedia.com/index.php?title=Rs2697962 reference = Chr12 snp rs2701175 119876054..119876054 "rs2701175 increases susceptibility to Type II Diabetes 1.33 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs2701175 reference = Chr5 snp rs27044 96144608..96144608 "rs27044 is one of several SNPs in the ARTS1 gene that has been shown in a large (over 1,000 Caucasia..." http://www.snpedia.com/index.php?title=Rs27044 reference = Chr5 illumina rs27048 1465645..1465645 "rs27048, a SNP in the dopamine transporter SLC6A3 gene, has been associated with more severe symptom..." http://www.snpedia.com/index.php?title=Rs27048 reference = Chr5 illumina rs27072 1447522..1447522 "rs27072, a SNP in the dopamine transporter SLC6A3 gene, has been associated with more severe symptom..." http://www.snpedia.com/index.php?title=Rs27072 reference = Chr7 illumina rs2710102 147205323..147205323 "rs2710102, a common SNP in the CNTNAP2 gene, was found to be significantly associated (p<0.028) with..." http://www.snpedia.com/index.php?title=Rs2710102 reference = Chr3 illumina rs2713604 129683149..129683149 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pgen.0020139 Th..." http://www.snpedia.com/index.php?title=Rs2713604 reference = Chr5 illumina rs272893 131690961..131690961 "rs272893 and rs273900 are associated with Crohn's disease (OR 2.16; 95% CI 1.21-3.59 and OR 2.40; 95..." http://www.snpedia.com/index.php?title=Rs272893 reference = Chr11 illumina rs2734849 112775370..112775370 "[http://scienceblogs.com/digitalbio/2008/06/a_receptor_for_dopamine_and_a.php blog] discussed in the..." http://www.snpedia.com/index.php?title=Rs2734849 reference = Chr19 illumina rs273506 18082647..18082647 "rs8108738 and rs273506 associated with Inflammatory bowel disease (P=1.8 x 10(-4))" http://www.snpedia.com/index.php?title=Rs273506 reference = Chr19 illumina rs2735839 56056435..56056435 "[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-g..." http://www.snpedia.com/index.php?title=Rs2735839 reference = Chr5 affy rs27388 126711708..126711708 "rs27388 is a SNP in the MEGF10 gene. In a case-control study involving 652 Irish patients, rs27388(A..." http://www.snpedia.com/index.php?title=Rs27388 reference = Chr5 snp rs273900 131722505..131722505 "rs272893 and rs273900 are associated with Crohn's disease (OR 2.16; 95% CI 1.21-3.59 and OR 2.40; 95..." http://www.snpedia.com/index.php?title=Rs273900 reference = Chr7 snp rs2740574 99220032..99220032 "rs2740574(G) alleles are associated with an ~10 fold higher risk of aggressive prostate cancer in Af..." http://www.snpedia.com/index.php?title=Rs2740574 reference = ChrY snp rs2740980 12942936..12942936 "" http://www.snpedia.com/index.php?title=Rs2740980 reference = ChrY illumina rs2740981 12943108..12943108 "" http://www.snpedia.com/index.php?title=Rs2740981 reference = Chr1 illumina rs2745557 184915844..184915844 "A study of 151 Korean families reported that the rs2745557(A) allele of the PTGS2 gene, also known a..." http://www.snpedia.com/index.php?title=Rs2745557 reference = Chr14 snp rs2754157 22957059..22957059 "" http://www.snpedia.com/index.php?title=Rs2754157 reference = Chr6 snp rs2758346 160035411..160035411 "rs2758346 rs4880 and rs2855116 association with Alzheimer's disease" http://www.snpedia.com/index.php?title=Rs2758346 reference = Chr1 both rs2773080 176963373..176963373 "Associated with type-2 diabetes in a Mexican-American population." http://www.snpedia.com/index.php?title=Rs2773080 reference = Chr1 both rs2774279 159284180..159284180 "The minor allele of rs2774279 was less common among individuals with metabolic syndrome than among h..." http://www.snpedia.com/index.php?title=Rs2774279 reference = Chr9 affy rs2779562 100317502..100317502 "Associated with nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs2779562 reference = Chr20 snp rs2787094 3597161..3597161 "rs2787094, a SNP in the ADAM33 gene, has been linked to a predisposition to asthma and bronchial hyp..." http://www.snpedia.com/index.php?title=Rs2787094 reference = Chr10 affy rs2789679 81897864..81897864 "499 German individuals with sarcoidosis and 490 controls; Validation in an independent sample 1,649 ..." http://www.snpedia.com/index.php?title=Rs2789679 reference = Chr1 snp rs2794521 157951720..157951720 "Associated with at least one 'mortality outcome' in a study of ~10,000 individuals." http://www.snpedia.com/index.php?title=Rs2794521 reference = Chr3 illumina rs279552 9951159..9951159 "" http://www.snpedia.com/index.php?title=Rs279552 reference = Chr4 snp rs279836 46033827..46033827 "This SNP in the GABRA2 gene has been linked to Alcoholism. The strongest association for this SNP is..." http://www.snpedia.com/index.php?title=Rs279836 reference = Chr4 affy rs279845 46024480..46024480 "This SNP in the GABRA2 gene has been linked to Alcoholism. The strongest association for this SNP is..." http://www.snpedia.com/index.php?title=Rs279845 reference = Chr4 illumina rs279858 46009350..46009350 "This SNP in the GABRA2 gene has been linked to Alcoholism. The effect of this SNP, a synonymous chan..." http://www.snpedia.com/index.php?title=Rs279858 reference = Chr4 snp rs279871 46000490..46000490 "This SNP in the GABRA2 gene has been linked to Alcoholism. The strongest association for this SNP is..." http://www.snpedia.com/index.php?title=Rs279871 reference = Chr6 snp rs2802292 109015211..109015211 "Discussed extensively at [http://scienceblogs.com/geneticfuture/2008/09/live_long_and_prosper_first_..." http://www.snpedia.com/index.php?title=Rs2802292 reference = Chr9 snp rs2808415 125165139..125165139 "" http://www.snpedia.com/index.php?title=Rs2808415 reference = Chr9 illumina rs2811712 21988035..21988035 "rs2811712 is a SNP associated with physical function in older individuals, and thus indirectly assoc..." http://www.snpedia.com/index.php?title=Rs2811712 reference = Chr1 illumina rs2814778 157441307..157441307 "rs2814778 is within the DARC gene, which encodes the Duffy blood group antigen . This SNP shows an a..." http://www.snpedia.com/index.php?title=Rs2814778 reference = Chr3 snp rs2819590 4483742..4483742 "" http://www.snpedia.com/index.php?title=Rs2819590 reference = Chr6 illumina rs2819861 45532918..45532918 "rs910586, rs2819861, and rs1934328 may influence cleft palate" http://www.snpedia.com/index.php?title=Rs2819861 reference = Chr1 affy rs2820037 237503165..237503165 "rs2820037 has been reported in a large study to be associated with high blood pressure. The risk all..." http://www.snpedia.com/index.php?title=Rs2820037 reference = Chr1 illumina rs2820312 200135880..200135880 "" http://www.snpedia.com/index.php?title=Rs2820312 reference = Chr21 illumina rs2822432 14438819..14438819 "" http://www.snpedia.com/index.php?title=Rs2822432 reference = Chr21 both rs2824721 18591989..18591989 "" http://www.snpedia.com/index.php?title=Rs2824721 reference = Chr21 snp rs2824790 18677911..18677911 "" http://www.snpedia.com/index.php?title=Rs2824790 reference = Chr21 snp rs2827196 22287002..22287002 "SNP rs2827196 has been associated with both diastolic blood pressure and systolic blood pressure in ..." http://www.snpedia.com/index.php?title=Rs2827196 reference = Chr4 illumina rs283413 100487213..100487213 "SNP rs283413, also known as G78stop, encodes a rare variant of the ADH1C gene that leads to a trunca..." http://www.snpedia.com/index.php?title=Rs283413 reference = Chr21 both rs2834167 33562658..33562658 "rs2834167 is a SNP in the interleukin-10 receptor 2 IL10RB gene. In a study of Japanese patients, rs..." http://www.snpedia.com/index.php?title=Rs2834167 reference = Chr7 snp rs28357225 27368981..27368981 "" http://www.snpedia.com/index.php?title=Rs28357225 reference = ChrNone snp rs28357980 4918..4918 "Also known as mitochondrial SNP 4917G. [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjourna..." http://www.snpedia.com/index.php?title=Rs28357980 reference = Chr5 snp rs28360071 82473898..82473898 "rs28360071 is an insertion/deletion SNP in the DNA repair XRCC4 gene. Individuals in a Taiwanese Chi..." http://www.snpedia.com/index.php?title=Rs28360071 reference = Chr21 illumina rs2836061 38247104..38247104 "This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients." http://www.snpedia.com/index.php?title=Rs2836061 reference = Chr1 illumina rs28362286 55301803..55301803 "[omim:LOW DENSITY LIPOPROTEIN CHOLESTEROL, LOW PLASMA LEVELS OF]" http://www.snpedia.com/index.php?title=Rs28362286 reference = Chr19 snp rs28362459 5795792..5795792 "[omim:Le(-) PHENOTYPE]" http://www.snpedia.com/index.php?title=Rs28362459 reference = Chr7 snp rs28362692 30918183..30918183 "[omim:COLTON BLOOD GROUP POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28362692 reference = Chr17 snp rs28365859 1250528..1250528 "In a Japanese population, SNP rs28365859 had higher minor (C) allele frequencies in controls (p(alle..." http://www.snpedia.com/index.php?title=Rs28365859 reference = Chr8 illumina rs28374544 106883455..106883455 "[omim:TETRALOGY OF FALLOT]" http://www.snpedia.com/index.php?title=Rs28374544 reference = Chr21 both rs2837960 41433788..41433788 "rs2837960 has been reported in a large study to be associated with rheumatoid arthritis. The risk al..." http://www.snpedia.com/index.php?title=Rs2837960 reference = Chr21 illumina rs2839110 46363388..46363388 "" http://www.snpedia.com/index.php?title=Rs2839110 reference = Chr21 both rs2839471 42427525..42427525 "500+ Japanese patients with high myopia were studied to reveal an association with the rs2839471(T) ..." http://www.snpedia.com/index.php?title=Rs2839471 reference = Chr11 snp rs2839698 1975429..1975429 "significantly decreased risk of bladder cancer was found for the rs2839698 TC genotype (odds ratio [..." http://www.snpedia.com/index.php?title=Rs2839698 reference = Chr19 snp rs28399447 46044781..46044781 "[omim:TEGAFUR, POOR METABOLISM OF]" http://www.snpedia.com/index.php?title=Rs28399447 reference = Chr10 illumina rs28399504 96512453..96512453 "rs28399504 is a SNP in the CYP2C19 gene, potentially encoding the CYP2C19*4 variant. This variant ha..." http://www.snpedia.com/index.php?title=Rs28399504 reference = Chr19 snp rs28399653 50007285..50007285 "[omim:LUTHERAN BLOOD GROUP POLYMORPHISM Lu(a)/Lu(b)]" http://www.snpedia.com/index.php?title=Rs28399653 reference = ChrNone snp rs28414810 1373457..1373457 "rs28414810, located in intron 8 of the CSF2RA gene, is part of a haplotype block that has been repor..." http://www.snpedia.com/index.php?title=Rs28414810 reference = Chr18 affy rs2848745 37311723..37311723 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs2848745 reference = ChrNone snp rs2852464 50996988..50996988 "" http://www.snpedia.com/index.php?title=Rs2852464 reference = Chr13 both rs2854344 47895694..47895694 "associated with breast cancer risk and ovarian cancer More specifically: carriers of two rs2854344..." http://www.snpedia.com/index.php?title=Rs2854344 reference = Chr6 illumina rs2855116 160026115..160026115 "rs2758346 rs4880 and rs2855116 association with Alzheimer's disease" http://www.snpedia.com/index.php?title=Rs2855116 reference = Chr6 illumina rs2858331 32789255..32789255 "Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature] Celiac diseased rs49..." http://www.snpedia.com/index.php?title=Rs2858331 reference = Chr19 snp rs2860174 7081718..7081718 "A combined study totaling 1,000+ patients with migraine susceptibility concluded that even larger nu..." http://www.snpedia.com/index.php?title=Rs2860174 reference = Chr3 illumina rs2863389 167631586..167631586 "rs2863389, rs7935082 and rs952635 implicated in type-2 diabetes by" http://www.snpedia.com/index.php?title=Rs2863389 reference = Chr4 illumina rs2866413 103776125..103776125 "" http://www.snpedia.com/index.php?title=Rs2866413 reference = ChrNone snp rs28694718 1374225..1374225 "rs28694718, located in intron 8 of the CSF2RA gene, is part of a haplotype block that has been repor..." http://www.snpedia.com/index.php?title=Rs28694718 reference = Chr22 snp rs2870984 17285859..17285859 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs2870984 reference = Chr11 snp rs28720026 18247456..18247456 "" http://www.snpedia.com/index.php?title=Rs28720026 reference = Chr1 affy rs287235 55451087..55451087 "The (G) allele of this snp has been implicated in a somewhat increased risk of developing late onset..." http://www.snpedia.com/index.php?title=Rs287235 reference = Chr4 snp rs28730619 100218248..100218248 "Genetic variation in GSNOR and childhood asthma. The name GSNOR is usually used in mice, for the hum..." http://www.snpedia.com/index.php?title=Rs28730619 reference = Chr17 snp rs28730837 53710396..53710396 "[omim:MYELOPEROXIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28730837 reference = Chr13 illumina rs287354 68137953..68137953 "SNP rs287354 has been associated with both cholesterol levels and low-density lipoprotein levels in ..." http://www.snpedia.com/index.php?title=Rs287354 reference = Chr13 snp rs287474 68173961..68173961 "SNP rs287474 has been associated with both cholesterol levels and low-density lipoprotein levels in ..." http://www.snpedia.com/index.php?title=Rs287474 reference = Chr14 snp rs28756986 74584242..74584242 "[omim:COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7]" http://www.snpedia.com/index.php?title=Rs28756986 reference = Chr6 illumina rs2881766 152160812..152160812 "rs2881766 is a SNP in the promoter region of the estrogen receptor alpha ESR1 gene. Carriers of rs28..." http://www.snpedia.com/index.php?title=Rs2881766 reference = Chr2 affy rs288326 183411581..183411581 "[omim:OSTEOARTHRITIS OF HIP, FEMALE-SPECIFIC, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs288326 reference = Chr17 illumina rs28897672 38512030..38512030 "[omim:OVARIAN CANCER, SPORADIC]" http://www.snpedia.com/index.php?title=Rs28897672 reference = Chr17 snp rs28903098 57292005..57292005 "[omim:BREAST CANCER, EARLY-ONSET]" http://www.snpedia.com/index.php?title=Rs28903098 reference = Chr9 affy rs2891168 22088619..22088619 "rs2891168 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AG) and ..." http://www.snpedia.com/index.php?title=Rs2891168 reference = Chr4 snp rs28928868 1777689..1777689 "[omim:HYPOCHONDROPLASIA]" http://www.snpedia.com/index.php?title=Rs28928868 reference = Chr4 snp rs28928869 1777684..1777684 "[omim:HYPOCHONDROPLASIA]" http://www.snpedia.com/index.php?title=Rs28928869 reference = Chr2 snp rs28928870 49044118..49044118 "[omim:OVARIAN HYPERSTIMULATION SYNDROME]" http://www.snpedia.com/index.php?title=Rs28928870 reference = Chr2 snp rs28928871 49043765..49043765 "[omim:OVARIAN HYPERSTIMULATION SYNDROME]" http://www.snpedia.com/index.php?title=Rs28928871 reference = Chr2 snp rs28928872 85632553..85632553 "[omim:VITAMIN K-DEPENDENT COAGULATION DEFECT]" http://www.snpedia.com/index.php?title=Rs28928872 reference = ChrX illumina rs28928873 120010039..120010039 "[omim:HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6]" http://www.snpedia.com/index.php?title=Rs28928873 reference = Chr3 snp rs28928874 172198782..172198782 "[omim:FANCONI-BICKEL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28928874 reference = Chr16 snp rs28928875 167055..167055 "[omim:HEMOGLOBIN Q (IRAN)]" http://www.snpedia.com/index.php?title=Rs28928875 reference = Chr16 snp rs28928876 167094..167094 "[omim:HEMOGLOBIN M (IWATE)]" http://www.snpedia.com/index.php?title=Rs28928876 reference = Chr16 snp rs28928877 167130..167130 "[omim:HEMOGLOBIN TURRIFF]" http://www.snpedia.com/index.php?title=Rs28928877 reference = Chr16 snp rs28928878 163207..163207 "[omim:HEMOGLOBIN ADANA]" http://www.snpedia.com/index.php?title=Rs28928878 reference = Chr16 snp rs28928879 167116..167116 "[omim:HEMOGLOBIN CAPA]" http://www.snpedia.com/index.php?title=Rs28928879 reference = Chr16 snp rs28928880 162985..162985 "[omim:HEMOGLOBIN RAMONA]" http://www.snpedia.com/index.php?title=Rs28928880 reference = Chr16 snp rs28928881 167351..167351 "[omim:HEMOGLOBIN MALHACEN]" http://www.snpedia.com/index.php?title=Rs28928881 reference = Chr16 snp rs28928882 167051..167051 "[omim:HEMOGLOBIN GOUDA]" http://www.snpedia.com/index.php?title=Rs28928882 reference = Chr16 snp rs28928883 163165..163165 "[omim:HEMOGLOBIN OITA]" http://www.snpedia.com/index.php?title=Rs28928883 reference = Chr16 snp rs28928884 167291..167291 "[omim:HEMOGLOBIN CHAROLLES]" http://www.snpedia.com/index.php?title=Rs28928884 reference = Chr16 snp rs28928885 162941..162941 "[omim:HEMOGLOBIN DELFZICHT]" http://www.snpedia.com/index.php?title=Rs28928885 reference = Chr16 snp rs28928886 163151..163151 "[omim:HEMOGLOBIN SARATOGA SPRINGS]" http://www.snpedia.com/index.php?title=Rs28928886 reference = Chr16 snp rs28928887 163211..163211 "[omim:HEMOGLOBIN J (BUDA)]" http://www.snpedia.com/index.php?title=Rs28928887 reference = Chr16 snp rs28928888 162913..162913 "[omim:ALPHA-THALASSEMIA]" http://www.snpedia.com/index.php?title=Rs28928888 reference = Chr16 snp rs28928889 163502..163502 "[omim:HEMOGLOBIN ANAMOSA]" http://www.snpedia.com/index.php?title=Rs28928889 reference = Chr4 snp rs28928890 4912778..4912778 "[omim:OROFACIAL CLEFT 5]" http://www.snpedia.com/index.php?title=Rs28928890 reference = Chr2 snp rs28928891 176667636..176667636 "[omim:BRACHYDACTYLY, TYPE E]" http://www.snpedia.com/index.php?title=Rs28928891 reference = Chr2 snp rs28928892 176667619..176667619 "[omim:BRACHYDACTYLY, TYPE E]" http://www.snpedia.com/index.php?title=Rs28928892 reference = Chr17 snp rs28928893 36996257..36996257 "[omim:EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE]" http://www.snpedia.com/index.php?title=Rs28928893 reference = Chr17 snp rs28928894 37022105..37022105 "[omim:PACHYONYCHIA CONGENITA, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28928894 reference = Chr17 snp rs28928895 37022084..37022084 "[omim:PACHYONYCHIA CONGENITA, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28928895 reference = Chr17 snp rs28928896 37034014..37034014 "During some blast and clustalw analysis of the watson genome, this snp is an outlier. It appears to ..." http://www.snpedia.com/index.php?title=Rs28928896 reference = Chr17 snp rs28928897 37034007..37034007 "[omim:PACHYONYCHIA CONGENITA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28928897 reference = Chr17 snp rs28928898 37034025..37034025 "[omim:PACHYONYCHIA CONGENITA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28928898 reference = Chr17 snp rs28928899 37034004..37034004 "[omim:PACHYONYCHIA CONGENITA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28928899 reference = Chr1 snp rs28928900 154351511..154351511 "[omim:CARDIOMYOPATHY, DILATED, 1A]" http://www.snpedia.com/index.php?title=Rs28928900 reference = Chr1 snp rs28928901 154371244..154371244 "[omim:EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28928901 reference = Chr1 snp rs28928902 154373366..154373366 "[omim:MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28928902 reference = Chr1 snp rs28928903 154351502..154351502 "[omim:WERNER SYNDROME, ATYPICAL]" http://www.snpedia.com/index.php?title=Rs28928903 reference = Chr7 snp rs28928904 150279636..150279636 "[omim:LONG QT SYNDROME 2]" http://www.snpedia.com/index.php?title=Rs28928904 reference = Chr7 snp rs28928905 150280535..150280535 "[omim:LONG QT SYNDROME, BRADYCARDIA-INDUCED]" http://www.snpedia.com/index.php?title=Rs28928905 reference = Chr15 illumina rs28928906 72976444..72976444 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib]" http://www.snpedia.com/index.php?title=Rs28928906 reference = Chr1 snp rs28928907 43576892..43576892 "[omim:AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28928907 reference = Chr1 snp rs28928908 43578354..43578354 "[omim:AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28928908 reference = Chr12 snp rs28928909 79625963..79625963 "[omim:MYOPATHY, CENTRONUCLEAR, MILD]" http://www.snpedia.com/index.php?title=Rs28928909 reference = Chr8 snp rs28928910 24869883..24869883 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E]" http://www.snpedia.com/index.php?title=Rs28928910 reference = Chr1 snp rs28929468 170615640..170615640 "[omim:AT-III ROUEN III]" http://www.snpedia.com/index.php?title=Rs28929468 reference = Chr1 snp rs28929469 172150556..172150556 "[omim:AT-III ROUEN IV]" http://www.snpedia.com/index.php?title=Rs28929469 reference = Chr14 snp rs28929470 93917139..93917139 "[omim:PI F]" http://www.snpedia.com/index.php?title=Rs28929470 reference = Chr14 snp rs28929471 93915598..93915598 "[omim:PI P(ST. ALBANS)]" http://www.snpedia.com/index.php?title=Rs28929471 reference = Chr14 snp rs28929472 93917039..93917039 "[omim:PI P(DUARTE)]" http://www.snpedia.com/index.php?title=Rs28929472 reference = Chr14 snp rs28929473 93914665..93914665 "[omim:PI NULL(MATTAWA)]" http://www.snpedia.com/index.php?title=Rs28929473 reference = Chr14 snp rs28929474 93914700..93914700 "[omim:PI Z(AUGSBURG)]" http://www.snpedia.com/index.php?title=Rs28929474 reference = ChrNone snp rs28929476 116213026..116213026 "[omim:APOLIPOPROTEIN A-I (BALTIMORE)]" http://www.snpedia.com/index.php?title=Rs28929476 reference = Chr12 snp rs28929477 48631179..48631179 "[omim:DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28929477 reference = Chr12 snp rs28929478 109204045..109204045 "[omim:DARIER DISEASE]" http://www.snpedia.com/index.php?title=Rs28929478 reference = Chr9 snp rs28929479 35782933..35782933 "[omim:ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE]" http://www.snpedia.com/index.php?title=Rs28929479 reference = Chr17 snp rs28929480 39693610..39693610 "[omim:SPHEROCYTOSIS, HEREDITARY, DUE TO BAND 3 CAPE TOWN]" http://www.snpedia.com/index.php?title=Rs28929480 reference = Chr10 snp rs28929481 50527621..50527621 "[omim:MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA]" http://www.snpedia.com/index.php?title=Rs28929481 reference = Chr10 snp rs28929482 50503686..50503686 "[omim:MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA]" http://www.snpedia.com/index.php?title=Rs28929482 reference = Chr2 snp rs28929483 47613920..47613920 "[omim:COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28929483 reference = Chr13 snp rs28929485 19661671..19661671 "[omim:KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME]" http://www.snpedia.com/index.php?title=Rs28929485 reference = Chr3 snp rs28929486 99792623..99792623 "[omim:COPROPORPHYRIA]" http://www.snpedia.com/index.php?title=Rs28929486 reference = Chr3 snp rs28929487 99787165..99787165 "[omim:COPROPORPHYRIA]" http://www.snpedia.com/index.php?title=Rs28929487 reference = Chr14 snp rs28929488 93840561..93840561 "[omim:CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28929488 reference = Chr11 snp rs28929489 111284868..111284868 "[omim:ALPHA-B CRYSTALLINOPATHY WITH CATARACT]" http://www.snpedia.com/index.php?title=Rs28929489 reference = Chr16 snp rs28929490 21177607..21177607 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC]" http://www.snpedia.com/index.php?title=Rs28929490 reference = Chr7 snp rs28929491 75257517..75257517 "[omim:POR DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28929491 reference = Chr4 snp rs28929492 88889288..88889288 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1]" http://www.snpedia.com/index.php?title=Rs28929492 reference = Chr19 snp rs28929493 806613..806613 "[omim:NEUTROPENIA, SEVERE CONGENITAL, AUTOSOMAL DOMINANT 1]" http://www.snpedia.com/index.php?title=Rs28929493 reference = Chr19 snp rs28929494 804338..804338 "[omim:NEUTROPENIA, SEVERE CONGENITAL, AUTOSOMAL DOMINANT 1]" http://www.snpedia.com/index.php?title=Rs28929494 reference = Chr7 snp rs28929495 55209201..55209201 "[omim:NONSMALL CELL LUNG CANCER, RESPONSE TO TYROSINE KINASE INHIBITOR IN, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28929495 reference = Chr13 snp rs28929496 102318550..102318550 "[omim:XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G]" http://www.snpedia.com/index.php?title=Rs28929496 reference = Chr1 snp rs28929497 194982990..194982990 "[omim:HEMOLYTIC UREMIC SYNDROME, ATYPICAL]" http://www.snpedia.com/index.php?title=Rs28929497 reference = Chr10 snp rs28929498 90763958..90763958 "[omim:SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28929498 reference = Chr10 snp rs28929499 90763919..90763919 "[omim:AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28929499 reference = Chr15 snp rs28929500 46576787..46576787 "[omim:MARFAN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28929500 reference = Chr15 snp rs28929501 46567970..46567970 "[omim:MARFAN SYNDROME, NEONATAL]" http://www.snpedia.com/index.php?title=Rs28929501 reference = Chr17 snp rs28929768 4746342..4746342 "[omim:MYASTHENIC SYNDROME, SLOW-CHANNEL CONGENITAL, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28929768 reference = Chr1 snp rs28930068 199289289..199289289 "[omim:HYPOKALEMIC PERIODIC PARALYSIS]" http://www.snpedia.com/index.php?title=Rs28930068 reference = Chr1 snp rs28930069 199289290..199289290 "[omim:HYPOKALEMIC PERIODIC PARALYSIS]" http://www.snpedia.com/index.php?title=Rs28930069 reference = Chr10 snp rs28930070 50526598..50526598 "[omim:MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA]" http://www.snpedia.com/index.php?title=Rs28930070 reference = Chr10 snp rs28930071 50498596..50498596 "[omim:MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA]" http://www.snpedia.com/index.php?title=Rs28930071 reference = Chr21 snp rs28930072 46242515..46242515 "[omim:BETHLEM MYOPATHY]" http://www.snpedia.com/index.php?title=Rs28930072 reference = Chr3 snp rs28930073 37023499..37023499 "[omim:COLORECTAL CANCER, SPORADIC, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs28930073 reference = Chr8 snp rs28930074 143991271..143991271 "[omim:CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28930074 reference = Chr2 snp rs28930075 220111709..220111709 "[omim:MYOPATHY, DESMIN-RELATED]" http://www.snpedia.com/index.php?title=Rs28930075 reference = Chr15 snp rs28930076 46516836..46516836 "[omim:MARFAN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28930076 reference = Chr20 snp rs28930970 42688571..42688571 "[omim:SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CE..." http://www.snpedia.com/index.php?title=Rs28930970 reference = Chr20 snp rs28930971 42687636..42687636 "[omim:SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CE..." http://www.snpedia.com/index.php?title=Rs28930971 reference = Chr20 snp rs28930972 42687648..42687648 "[omim:ADENOSINE DEAMINASE DEFICIENCY, PARTIAL]" http://www.snpedia.com/index.php?title=Rs28930972 reference = Chr20 snp rs28930973 42684966..42684966 "[omim:ADENOSINE DEAMINASE DEFICIENCY, PARTIAL]" http://www.snpedia.com/index.php?title=Rs28930973 reference = Chr9 snp rs28930974 127710288..127710288 "[omim:ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO]" http://www.snpedia.com/index.php?title=Rs28930974 reference = Chr4 snp rs28930975 74644289..74644289 "[omim:ALBUMIN ROMA]" http://www.snpedia.com/index.php?title=Rs28930975 reference = Chr4 snp rs28930976 74645819..74645819 "[omim:ALBUMIN IOWA CITY 1]" http://www.snpedia.com/index.php?title=Rs28930976 reference = Chr14 snp rs28930977 72755653..72755653 "Variations in this snp are related to ALZHEIMER DISEASE, FAMILIAL, 3 [http://www.ncbi.nlm.nih.gov/en..." http://www.snpedia.com/index.php?title=Rs28930977 reference = Chr1 snp rs28930978 170604833..170604833 "[omim:AT-III CHARLEVILLE]" http://www.snpedia.com/index.php?title=Rs28930978 reference = Chr14 snp rs28931568 93919056..93919056 "[omim:PI M(MINERAL SPRINGS)]" http://www.snpedia.com/index.php?title=Rs28931568 reference = Chr14 snp rs28931569 93919134..93919134 "[omim:PI M(PROCIDA)]" http://www.snpedia.com/index.php?title=Rs28931569 reference = Chr14 snp rs28931570 93919141..93919141 "[omim:PI I]" http://www.snpedia.com/index.php?title=Rs28931570 reference = Chr14 snp rs28931572 93918981..93918981 "[omim:PI NULL(LUDWIGSHAFEN)]" http://www.snpedia.com/index.php?title=Rs28931572 reference = ChrNone snp rs28931573 116211949..116211949 "[omim:APOLIPOPROTEIN A-I (MILANO)]" http://www.snpedia.com/index.php?title=Rs28931573 reference = ChrNone snp rs28931574 116212979..116212979 "[omim:AMYLOID POLYNEUROPATHY-NEPHROPATHY, IOWA TYPE]" http://www.snpedia.com/index.php?title=Rs28931574 reference = ChrNone snp rs28931575 116212197..116212197 "[omim:AMYLOIDOSIS, CARDIAC AND CUTANEOUS]" http://www.snpedia.com/index.php?title=Rs28931575 reference = Chr19 snp rs28931576 50102991..50102991 "[omim:APOE3(-)-FREIBURG]" http://www.snpedia.com/index.php?title=Rs28931576 reference = Chr19 snp rs28931577 50103742..50103742 "[omim:APOE3 VARIANT]" http://www.snpedia.com/index.php?title=Rs28931577 reference = Chr19 snp rs28931578 50103848..50103848 "[omim:APOE2 VARIANT]" http://www.snpedia.com/index.php?title=Rs28931578 reference = Chr19 snp rs28931579 50104333..50104333 "[omim:APOE4(+)]" http://www.snpedia.com/index.php?title=Rs28931579 reference = Chr12 snp rs28931580 48631050..48631050 "[omim:DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28931580 reference = Chr9 snp rs28931581 35782499..35782499 "[omim:ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE]" http://www.snpedia.com/index.php?title=Rs28931581 reference = Chr9 snp rs28931582 35782748..35782748 "[omim:ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE]" http://www.snpedia.com/index.php?title=Rs28931582 reference = Chr17 snp rs28931583 39691414..39691414 "[omim:SPHEROCYTOSIS, HEREDITARY, DUE TO BAND 3 TUSCALOOSA]" http://www.snpedia.com/index.php?title=Rs28931583 reference = Chr17 snp rs28931584 39690408..39690408 "[omim:SPHEROCYTOSIS, HEREDITARY]" http://www.snpedia.com/index.php?title=Rs28931584 reference = Chr17 snp rs28931585 39684100..39684100 "[omim:SPHEROCYTOSIS, HEREDITARY, DUE TO BAND 3 PRAGUE III]" http://www.snpedia.com/index.php?title=Rs28931585 reference = Chr20 snp rs28931586 44184395..44184395 "[omim:IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 3]" http://www.snpedia.com/index.php?title=Rs28931586 reference = Chr3 snp rs28931588 41241101..41241101 "[omim:PILOMATRICOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28931588 reference = Chr3 snp rs28931589 41241108..41241108 "[omim:HEPATOBLASTOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28931589 reference = Chr19 snp rs28931590 38484910..38484910 "[omim:LEUKEMIA, ACUTE MYELOID]" http://www.snpedia.com/index.php?title=Rs28931590 reference = Chr20 snp rs28931591 61452356..61452356 "[omim:EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28931591 reference = Chr13 snp rs28931592 19661245..19661245 "[omim:DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 1]" http://www.snpedia.com/index.php?title=Rs28931592 reference = Chr13 snp rs28931593 19661497..19661497 "[omim:KERATODERMA, PALMOPLANTAR, WITH DEAFNESS]" http://www.snpedia.com/index.php?title=Rs28931593 reference = Chr13 snp rs28931594 19661573..19661573 "[omim:KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME]" http://www.snpedia.com/index.php?title=Rs28931594 reference = Chr13 snp rs28931595 19661186..19661186 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 3]" http://www.snpedia.com/index.php?title=Rs28931595 reference = Chr5 snp rs28931596 108416008..108416008 "[omim:OCULODENTODIGITAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28931596 reference = Chr5 snp rs28931597 108416006..108416006 "[omim:OCULODENTODIGITAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28931597 reference = Chr5 snp rs28931598 108415997..108415997 "[omim:OCULODENTODIGITAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28931598 reference = Chr5 snp rs28931599 108415993..108415993 "[omim:OCULODENTODIGITAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28931599 reference = Chr6 snp rs28931600 121810119..121810119 "[omim:SYNDACTYLY, TYPE III]" http://www.snpedia.com/index.php?title=Rs28931600 reference = Chr6 illumina rs28931601 121809978..121809978 "[omim:OCULODENTODIGITAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28931601 reference = Chr5 snp rs28931602 127699134..127699134 "[omim:CONTRACTURAL ARACHNODACTYLY, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28931602 reference = Chr3 snp rs28931603 99782243..99782243 "[omim:COPROPORPHYRIA]" http://www.snpedia.com/index.php?title=Rs28931603 reference = Chr2 illumina rs28931604 208701195..208701195 "[omim:CATARACT, CONGENITAL LAMELLAR]" http://www.snpedia.com/index.php?title=Rs28931604 reference = Chr2 snp rs28931605 208697263..208697263 "[omim:CATARACT, CONGENITAL LAMELLAR]" http://www.snpedia.com/index.php?title=Rs28931605 reference = Chr7 snp rs28931606 75452909..75452909 "[omim:POR DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28931606 reference = Chr7 snp rs28931607 75453213..75453213 "[omim:DISORDERED STEROIDOGENESIS, ISOLATED]" http://www.snpedia.com/index.php?title=Rs28931607 reference = Chr7 snp rs28931608 75452433..75452433 "[omim:POR DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28931608 reference = Chr8 snp rs28931609 143993518..143993518 "[omim:CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28931609 reference = Chr6 snp rs28931610 7529590..7529590 "[omim:SKIN FRAGILITY-WOOLLY HAIR SYNDROME]" http://www.snpedia.com/index.php?title=Rs28931610 reference = Chr19 snp rs28931611 804019..804019 "[omim:NEUTROPENIA, SEVERE CONGENITAL, AUTOSOMAL DOMINANT 1]" http://www.snpedia.com/index.php?title=Rs28931611 reference = Chr11 snp rs28931612 64334082..64334082 "[omim:PARATHYROID ADENOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28931612 reference = Chr22 illumina rs28931613 49314874..49314874 "[omim:MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28931613 reference = Chr4 snp rs28931614 1775917..1775917 "[omim:ACHONDROPLASIA]" http://www.snpedia.com/index.php?title=Rs28931614 reference = Chr4 snp rs28931615 1775951..1775951 "[omim:CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS]" http://www.snpedia.com/index.php?title=Rs28931615 reference = Chr5 illumina rs28932178 176570182..176570182 "" http://www.snpedia.com/index.php?title=Rs28932178 reference = Chr2 snp rs28932472 25237552..25237552 "[omim:OBESITY, EARLY-ONSET, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs28932472 reference = Chr17 snp rs28932768 40344171..40344171 "[omim:ALEXANDER DISEASE]" http://www.snpedia.com/index.php?title=Rs28932768 reference = Chr17 snp rs28932769 40344202..40344202 "[omim:ALEXANDER DISEASE]" http://www.snpedia.com/index.php?title=Rs28932769 reference = Chr19 snp rs28932770 61523235..61523235 "[omim:DIABETES MELLITUS, TYPE II]" http://www.snpedia.com/index.php?title=Rs28932770 reference = Chr5 snp rs28932771 86680877..86680877 "[omim:BASAL CELL CARCINOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28932771 reference = Chr5 snp rs28932772 86680885..86680885 "[omim:BASAL CELL CARCINOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28932772 reference = Chr17 snp rs28932773 10250966..10250966 "[omim:CARNEY COMPLEX VARIANT]" http://www.snpedia.com/index.php?title=Rs28932773 reference = Chr12 snp rs28932774 109819669..109819669 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10]" http://www.snpedia.com/index.php?title=Rs28932774 reference = Chr7 snp rs28932775 116016032..116016032 "[omim:RENAL CELL CARCINOMA, PAPILLARY, 2]" http://www.snpedia.com/index.php?title=Rs28932775 reference = Chr7 snp rs28932776 116017334..116017334 "[omim:RENAL CELL CARCINOMA, PAPILLARY, 2]" http://www.snpedia.com/index.php?title=Rs28932776 reference = Chr7 snp rs28932777 116017358..116017358 "[omim:RENAL CELL CARCINOMA, PAPILLARY, 2]" http://www.snpedia.com/index.php?title=Rs28932777 reference = Chr7 snp rs28932778 116016053..116016053 "[omim:RENAL CELL CARCINOMA, PAPILLARY, SPORADIC]" http://www.snpedia.com/index.php?title=Rs28932778 reference = Chr4 snp rs28933068 1777169..1777169 "[omim:HYPOCHONDROPLASIA]" http://www.snpedia.com/index.php?title=Rs28933068 reference = Chr1 snp rs28933069 237997984..237997984 "[omim:LEIOMYOMATOSIS AND RENAL CELL CANCER]" http://www.snpedia.com/index.php?title=Rs28933069 reference = Chr5 snp rs28933070 161453549..161453549 "[omim:EPILEPSY, CHILDHOOD ABSENCE, 2]" http://www.snpedia.com/index.php?title=Rs28933070 reference = Chr17 snp rs28933071 40344645..40344645 "[omim:ALEXANDER DISEASE]" http://www.snpedia.com/index.php?title=Rs28933071 reference = Chr5 snp rs28933072 151211241..151211241 "[omim:HYPEREKPLEXIA, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28933072 reference = Chr5 snp rs28933073 151211279..151211279 "[omim:HYPEREKPLEXIA, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28933073 reference = Chr4 snp rs28933074 68288929..68288929 "[omim:HYPOGONADOTROPIC HYPOGONADISM]" http://www.snpedia.com/index.php?title=Rs28933074 reference = Chr3 snp rs28933075 50268698..50268698 "[omim:PITUITARY ADENOMA, ACTH-SECRETING]" http://www.snpedia.com/index.php?title=Rs28933075 reference = Chr11 snp rs28933076 5211817..5211817 "[omim:HEMOGLOBIN A(2) WRENS]" http://www.snpedia.com/index.php?title=Rs28933076 reference = Chr11 illumina rs28933077 5211832..5211832 "[omim:HEMOGLOBIN A(2) SANT' ANTIOCO]" http://www.snpedia.com/index.php?title=Rs28933077 reference = Chr11 snp rs28933078 5227311..5227311 "[omim:HEMOGLOBIN F (SACROMONTE)]" http://www.snpedia.com/index.php?title=Rs28933078 reference = Chr11 illumina rs28933080 5231172..5231172 "[omim:HEMOGLOBIN F (CALABRIA)]" http://www.snpedia.com/index.php?title=Rs28933080 reference = Chr4 snp rs28933081 4912892..4912892 "[omim:OROFACIAL CLEFT 5]" http://www.snpedia.com/index.php?title=Rs28933081 reference = Chr2 snp rs28933082 176667588..176667588 "[omim:SYNPOLYDACTYLY 1]" http://www.snpedia.com/index.php?title=Rs28933082 reference = Chr19 snp rs28933083 7121572..7121572 "[omim:DONOHUE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28933083 reference = Chr19 snp rs28933084 7073673..7073673 "[omim:DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS]" http://www.snpedia.com/index.php?title=Rs28933084 reference = Chr19 snp rs28933085 7121565..7121565 "[omim:DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS]" http://www.snpedia.com/index.php?title=Rs28933085 reference = Chr19 snp rs28933086 7071688..7071688 "[omim:DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS]" http://www.snpedia.com/index.php?title=Rs28933086 reference = Chr12 snp rs28933087 51172720..51172720 "[omim:PACHYONYCHIA CONGENITA, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28933087 reference = Chr17 snp rs28933088 37033996..37033996 "[omim:PACHYONYCHIA CONGENITA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28933088 reference = Chr17 snp rs28933089 37033992..37033992 "[omim:PACHYONYCHIA CONGENITA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28933089 reference = Chr1 illumina rs28933090 154351587..154351587 "[omim:CARDIOMYOPATHY, DILATED, 1A]" http://www.snpedia.com/index.php?title=Rs28933090 reference = Chr1 snp rs28933091 152917338..152917338 "[omim:CARDIOMYOPATHY, DILATED, 1A]" http://www.snpedia.com/index.php?title=Rs28933091 reference = Chr1 snp rs28933092 154370912..154370912 "[omim:CARDIOMYOPATHY, DILATED, 1A]" http://www.snpedia.com/index.php?title=Rs28933092 reference = Chr1 snp rs28933093 152913605..152913605 "[omim:CARDIOMYOPATHY, DILATED, 1A]" http://www.snpedia.com/index.php?title=Rs28933093 reference = Chr15 snp rs28933094 56643040..56643040 "[omim:HEPATIC LIPASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933094 reference = Chr7 snp rs28933095 150109561..150109561 "[omim:LONG QT SYNDROME 2]" http://www.snpedia.com/index.php?title=Rs28933095 reference = Chr6 snp rs28933096 129553155..129553155 "[omim:MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933096 reference = Chr1 snp rs28933097 233374543..233374543 "[omim:METHYLCOBALAMIN DEFICIENCY, cblG TYPE]" http://www.snpedia.com/index.php?title=Rs28933097 reference = Chr14 snp rs28933098 22954070..22954070 "[omim:MYOPATHY, MYOSIN STORAGE]" http://www.snpedia.com/index.php?title=Rs28933098 reference = Chr12 snp rs28933099 109814811..109814811 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10]" http://www.snpedia.com/index.php?title=Rs28933099 reference = Chr14 snp rs28933100 34943507..34943507 "[omim:ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28933100 reference = Chr7 snp rs28933101 116012832..116012832 "[omim:RENAL CELL CARCINOMA, PAPILLARY, 2]" http://www.snpedia.com/index.php?title=Rs28933101 reference = Chr17 snp rs28933368 35135500..35135500 "[omim:GLIOBLASTOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28933368 reference = Chr17 snp rs28933369 35134523..35134523 "[omim:GASTRIC CANCER, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28933369 reference = Chr17 illumina rs28933370 35134904..35134904 "[omim:OVARIAN CARCINOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28933370 reference = Chr4 snp rs28933371 55288442..55288442 "[omim:PIEBALDISM]" http://www.snpedia.com/index.php?title=Rs28933371 reference = Chr7 snp rs28933372 41972396..41972396 "[omim:ACROCALLOSAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28933372 reference = Chr14 snp rs28933373 36202119..36202119 "[omim:TOOTH AGENESIS, SELECTIVE, 3]" http://www.snpedia.com/index.php?title=Rs28933373 reference = Chr10 snp rs28933374 72028449..72028449 "[omim:HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28933374 reference = Chr10 snp rs28933375 72028728..72028728 "[omim:HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28933375 reference = Chr10 snp rs28933376 72028179..72028179 "[omim:HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28933376 reference = Chr3 snp rs28933377 130263439..130263439 "[omim:BERNARD-SOULIER SYNDROME, TYPE C]" http://www.snpedia.com/index.php?title=Rs28933377 reference = Chr3 snp rs28933378 130263342..130263342 "[omim:BERNARD-SOULIER SYNDROME, TYPE C]" http://www.snpedia.com/index.php?title=Rs28933378 reference = Chr5 snp rs28933379 112202549..112202549 "[omim:GASTRIC CANCER, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28933379 reference = Chr12 snp rs28933381 4891529..4891529 "[omim:MYOKYMIA]" http://www.snpedia.com/index.php?title=Rs28933381 reference = Chr12 snp rs28933382 4891536..4891536 "[omim:MYOKYMIA]" http://www.snpedia.com/index.php?title=Rs28933382 reference = Chr12 snp rs28933383 4891482..4891482 "[omim:EPISODIC ATAXIA, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28933383 reference = Chr21 snp rs28933384 34743783..34743783 "[omim:JERVELL AND LANGE-NIELSEN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28933384 reference = Chr20 snp rs28933385 4628464..4628464 "[omim:CREUTZFELDT-JAKOB DISEASE]" http://www.snpedia.com/index.php?title=Rs28933385 reference = Chr6 snp rs28933386 138069122..138069122 "[omim:NOONAN SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28933386 reference = Chr3 snp rs28933388 108308312..108308312 "[omim:LEUKEMIA, JUVENILE MYELOMONOCYTIC]" http://www.snpedia.com/index.php?title=Rs28933388 reference = Chr3 snp rs28933389 167030704..167030704 "[omim:BCHE, FLUORIDE 1]" http://www.snpedia.com/index.php?title=Rs28933389 reference = Chr3 snp rs28933390 167030263..167030263 "[omim:BCHE, FLUORIDE 2]" http://www.snpedia.com/index.php?title=Rs28933390 reference = Chr3 illumina rs28933391 58388851..58388851 "[omim:PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933391 reference = Chr11 snp rs28933392 36553594..36553594 "[omim:SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE]" http://www.snpedia.com/index.php?title=Rs28933392 reference = Chr3 snp rs28933394 130730439..130730439 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933394 reference = Chr3 snp rs28933395 130730424..130730424 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933395 reference = Chr19 snp rs28933396 43682477..43682477 "[omim:CENTRAL CORE DISEASE]" http://www.snpedia.com/index.php?title=Rs28933396 reference = Chr19 snp rs28933397 43683134..43683134 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28933397 reference = Chr1 snp rs28933398 158372259..158372259 "[omim:MIGRAINE, FAMILIAL HEMIPLEGIC, 2]" http://www.snpedia.com/index.php?title=Rs28933398 reference = Chr1 snp rs28933399 158373079..158373079 "[omim:MIGRAINE, FAMILIAL HEMIPLEGIC, 2]" http://www.snpedia.com/index.php?title=Rs28933399 reference = Chr1 snp rs28933400 158371924..158371924 "[omim:MIGRAINE, FAMILIAL HEMIPLEGIC, 2]" http://www.snpedia.com/index.php?title=Rs28933400 reference = Chr1 snp rs28933401 158371660..158371660 "[omim:MIGRAINE, FAMILIAL HEMIPLEGIC, 2]" http://www.snpedia.com/index.php?title=Rs28933401 reference = Chr9 illumina rs28933402 135210569..135210569 "[omim:LEIGH SYNDROME DUE TO CYTOCHROME c OXIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933402 reference = Chr2 snp rs28933405 179358971..179358971 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9]" http://www.snpedia.com/index.php?title=Rs28933405 reference = Chr11 snp rs28933406 523875..523875 "[omim:THYROID CARCINOMA, FOLLICULAR, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28933406 reference = Chr8 snp rs28933407 128819859..128819859 "[omim:BURKITT LYMPHOMA]" http://www.snpedia.com/index.php?title=Rs28933407 reference = Chr3 snp rs28933408 24139408..24139408 "[omim:THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28933408 reference = ChrX snp rs28933668 153847991..153847991 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933668 reference = ChrX snp rs28933669 153847992..153847992 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933669 reference = ChrX snp rs28933670 153847952..153847952 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933670 reference = ChrX snp rs28933671 153847940..153847940 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933671 reference = ChrX snp rs28933672 153847589..153847589 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933672 reference = ChrX snp rs28933673 153812090..153812090 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933673 reference = ChrX snp rs28933674 153786340..153786340 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933674 reference = ChrX snp rs28933675 153786336..153786336 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933675 reference = ChrX snp rs28933676 153786333..153786333 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933676 reference = ChrX snp rs28933677 153786308..153786308 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933677 reference = ChrX snp rs28933678 153785987..153785987 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933678 reference = ChrX snp rs28933679 153785980..153785980 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933679 reference = ChrX snp rs28933680 153785962..153785962 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933680 reference = ChrX illumina rs28933681 153785870..153785870 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933681 reference = ChrX snp rs28933682 153785551..153785551 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28933682 reference = ChrX snp rs28933683 152789503..152789503 "[omim:MASA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28933683 reference = ChrX snp rs28933684 43694021..43694021 "[omim:EXUDATIVE VITREORETINOPATHY, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28933684 reference = ChrX snp rs28933685 43702835..43702835 "[omim:NORRIE DISEASE]" http://www.snpedia.com/index.php?title=Rs28933685 reference = ChrX snp rs28933686 67207584..67207584 "[omim:PHOSPHOGLYCERATE KINASE 1 DEFICIENCY, HAMAMATSU]" http://www.snpedia.com/index.php?title=Rs28933686 reference = ChrX illumina rs28933687 46598105..46598105 "[omim:RETINITIS PIGMENTOSA 2, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28933687 reference = ChrX snp rs28933688 105167309..105167309 "[omim:THYROXINE-BINDING GLOBULIN DEFICIENCY, PARTIAL, MONTREAL TYPE]" http://www.snpedia.com/index.php?title=Rs28933688 reference = ChrX snp rs28933689 105167359..105167359 "[omim:THYROXINE-BINDING GLOBULIN DEFICIENCY, PARTIAL, GARY TYPE]" http://www.snpedia.com/index.php?title=Rs28933689 reference = ChrX illumina rs28933690 37472199..37472199 "[omim:MCLEOD SYNDROME]" http://www.snpedia.com/index.php?title=Rs28933690 reference = ChrX snp rs28933691 47659525..47659525 "[omim:MENTAL RETARDATION, X-LINKED 45]" http://www.snpedia.com/index.php?title=Rs28933691 reference = Chr9 snp rs28933692 106620932..106620932 "[omim:HIGH DENSITY LIPOPROTEIN DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933692 reference = Chr17 snp rs28933693 45600013..45600013 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D]" http://www.snpedia.com/index.php?title=Rs28933693 reference = Chr17 snp rs28933694 45600758..45600758 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D]" http://www.snpedia.com/index.php?title=Rs28933694 reference = Chr17 snp rs28933695 7858742..7858742 "[omim:CONE-ROD DYSTROPHY 6]" http://www.snpedia.com/index.php?title=Rs28933695 reference = Chr19 snp rs28933696 15163945..15163945 "[omim:CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28933696 reference = Chr19 snp rs28933697 15163906..15163906 "[omim:CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28933697 reference = Chr19 snp rs28933698 15160815..15160815 "[omim:CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28933698 reference = Chr19 snp rs28933699 18757853..18757853 "[omim:PSEUDOACHONDROPLASIA]" http://www.snpedia.com/index.php?title=Rs28933699 reference = Chr4 snp rs28933969 55440248..55440248 "[omim:GERM CELL TUMOR]" http://www.snpedia.com/index.php?title=Rs28933969 reference = Chr14 snp rs28933970 36201910..36201910 "[omim:TOOTH AGENESIS, SELECTIVE, 3]" http://www.snpedia.com/index.php?title=Rs28933970 reference = Chr14 snp rs28933971 36201931..36201931 "[omim:TOOTH AGENESIS, SELECTIVE, 3]" http://www.snpedia.com/index.php?title=Rs28933971 reference = Chr14 snp rs28933972 36201924..36201924 "[omim:TOOTH AGENESIS, SELECTIVE, 3]" http://www.snpedia.com/index.php?title=Rs28933972 reference = Chr10 snp rs28933973 72028810..72028810 "[omim:HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28933973 reference = Chr1 snp rs28933974 21634957..21634957 "[omim:HYPOPHOSPHATASIA]" http://www.snpedia.com/index.php?title=Rs28933974 reference = Chr1 snp rs28933975 21634934..21634934 "[omim:ODONTOHYPOPHOSPHATASIA]" http://www.snpedia.com/index.php?title=Rs28933975 reference = Chr7 snp rs28933976 55863021..55863021 "[omim:PHOSPHOSERINE PHOSPHATASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933976 reference = Chr6 snp rs28933977 132247772..132247772 "[omim:ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY]" http://www.snpedia.com/index.php?title=Rs28933977 reference = Chr17 snp rs28933978 59804699..59804699 "[omim:PLATELET-ENDOTHELIAL CELL ADHESION MOLECULE 1 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28933978 reference = Chr18 snp rs28933979 27426935..27426935 "[omim:AMYLOID POLYNEUROPATHY, ANDRADE OR PORTUGUESE TYPE]" http://www.snpedia.com/index.php?title=Rs28933979 reference = Chr18 snp rs28933980 27432616..27432616 "[omim:AMYLOIDOSIS, SENILE]" http://www.snpedia.com/index.php?title=Rs28933980 reference = Chr18 snp rs28933981 27432608..27432608 "[omim:PREALBUMIN CHICAGO]" http://www.snpedia.com/index.php?title=Rs28933981 reference = Chr18 snp rs28933982 27432578..27432578 "[omim:HYPERTHYROXINEMIA, FAMILIAL DYSPREALBUMINEMIC EUTHYROID]" http://www.snpedia.com/index.php?title=Rs28933982 reference = Chr18 snp rs28933983 27429131..27429131 "[omim:AMYLOIDOSIS, OCULOLEPTOMENINGEAL]" http://www.snpedia.com/index.php?title=Rs28933983 reference = Chr1 snp rs28933984 59238249..59238249 "[omim:BREAST CANCER, SPORADIC]" http://www.snpedia.com/index.php?title=Rs28933984 reference = Chr11 illumina rs28933985 2137725..2137725 "[omim:HYPERPROINSULINEMIA, FAMILIAL]" http://www.snpedia.com/index.php?title=Rs28933985 reference = Chr2 snp rs28933986 127899986..127899986 "[omim:PROTEIN C DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933986 reference = Chr2 snp rs28933987 127899987..127899987 "[omim:PROTEIN C DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28933987 reference = Chr15 snp rs28933988 41294681..41294681 "[omim:SPHEROCYTOSIS, HEREDITARY, JAPANESE TYPE]" http://www.snpedia.com/index.php?title=Rs28933988 reference = Chr15 snp rs28933989 87559368..87559368 "[omim:RETINITIS PIGMENTOSA, RLBP1-RELATED]" http://www.snpedia.com/index.php?title=Rs28933989 reference = Chr15 snp rs28933990 87555029..87555029 "[omim:BOTHNIA RETINAL DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28933990 reference = Chr6 snp rs28933991 49688178..49688178 "[omim:RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE]" http://www.snpedia.com/index.php?title=Rs28933991 reference = Chr3 snp rs28933992 130733829..130733829 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933992 reference = Chr3 snp rs28933993 130733885..130733885 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933993 reference = Chr3 snp rs28933994 130730590..130730590 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933994 reference = Chr3 snp rs28933995 130733881..130733881 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs28933995 reference = Chr19 snp rs28933996 43640025..43640025 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28933996 reference = Chr19 snp rs28933997 43631192..43631192 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28933997 reference = Chr19 snp rs28933998 43677044..43677044 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28933998 reference = Chr19 snp rs28933999 43677045..43677045 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28933999 reference = Chr19 snp rs28934000 43678763..43678763 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28934000 reference = Chr19 snp rs28934001 43686799..43686799 "[omim:MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1]" http://www.snpedia.com/index.php?title=Rs28934001 reference = Chr1 snp rs28934002 158365181..158365181 "[omim:ALTERNATING HEMIPLEGIA OF CHILDHOOD]" http://www.snpedia.com/index.php?title=Rs28934002 reference = Chr2 snp rs28934003 166608720..166608720 "Possible [http://www.gtg.com.au/HumanDNATesting/index.asp?menuid=070.020.050.010 commercial test] [..." http://www.snpedia.com/index.php?title=Rs28934003 reference = Chr1 snp rs28934004 155468152..155468152 "[omim:ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE]" http://www.snpedia.com/index.php?title=Rs28934004 reference = Chr1 snp rs28934005 155468153..155468153 "[omim:ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE]" http://www.snpedia.com/index.php?title=Rs28934005 reference = Chr14 snp rs28934006 64359565..64359565 "[omim:ELLIPTOCYTOSIS DUE TO SPECTRIN PROMISSAO]" http://www.snpedia.com/index.php?title=Rs28934006 reference = Chr19 snp rs28934268 46539960..46539960 "[omim:CAMURATI-ENGELMANN DISEASE]" http://www.snpedia.com/index.php?title=Rs28934268 reference = Chr15 snp rs28934269 61140167..61140167 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3]" http://www.snpedia.com/index.php?title=Rs28934269 reference = Chr15 snp rs28934270 61140151..61140151 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3]" http://www.snpedia.com/index.php?title=Rs28934270 reference = Chr17 snp rs28934271 7517597..7517597 "[omim:LI-FRAUMENI SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934271 reference = Chr15 snp rs28934272 25903842..25903842 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934272 reference = Chr8 snp rs28934273 17966290..17966290 "[omim:FARBER LIPOGRANULOMATOSIS]" http://www.snpedia.com/index.php?title=Rs28934273 reference = Chr3 snp rs28934274 33085345..33085345 "[omim:GM1-GANGLIOSIDOSIS, INFANTILE TYPE]" http://www.snpedia.com/index.php?title=Rs28934274 reference = Chr21 snp rs28934275 43357110..43357110 "[omim:HOMOCYSTINURIA, PYRIDOXINE-RESPONSIVE]" http://www.snpedia.com/index.php?title=Rs28934275 reference = Chr12 snp rs28934276 101749073..101749073 "[omim:PHENYLKETONURIA]" http://www.snpedia.com/index.php?title=Rs28934276 reference = Chr16 snp rs28934277 70161298..70161298 "[omim:TYROSINEMIA, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934277 reference = Chr3 snp rs28934568 30688602..30688602 "[omim:MARFAN SYNDROME, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934568 reference = ChrNone snp rs28934569 76938376..76938376 "[omim:TRIOSEPHOSPHATE ISOMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934569 reference = Chr1 snp rs28934570 76938186..76938186 "[omim:TRIOSEPHOSPHATE ISOMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934570 reference = Chr17 snp rs28934571 7518259..7518259 "[omim:HEPATOCELLULAR CARCINOMA]" http://www.snpedia.com/index.php?title=Rs28934571 reference = Chr17 snp rs28934572 7518275..7518275 "[omim:LI-FRAUMENI SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28934572 reference = Chr17 snp rs28934573 7518284..7518284 "[omim:HEPATOBLASTOMA]" http://www.snpedia.com/index.php?title=Rs28934573 reference = Chr17 snp rs28934574 7517819..7517819 "[omim:OSTEOSARCOMA]" http://www.snpedia.com/index.php?title=Rs28934574 reference = Chr17 snp rs28934575 7518273..7518273 "[omim:OSTEOSARCOMA]" http://www.snpedia.com/index.php?title=Rs28934575 reference = Chr17 snp rs28934576 7517845..7517845 "[omim:LI-FRAUMENI SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934576 reference = Chr17 snp rs28934577 7518236..7518236 "[omim:MULTIPLE MALIGNANCY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934577 reference = Chr17 snp rs28934578 7519131..7519131 "[omim:LI-FRAUMENI SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28934578 reference = Chr11 snp rs28934579 2145955..2145955 "[omim:SEGAWA SYNDROME, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28934579 reference = Chr11 snp rs28934580 2144499..2144499 "[omim:SEGAWA SYNDROME, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28934580 reference = Chr11 snp rs28934581 2144801..2144801 "[omim:SEGAWA SYNDROME, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28934581 reference = Chr16 snp rs28934582 20267681..20267681 "[omim:HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE]" http://www.snpedia.com/index.php?title=Rs28934582 reference = Chr16 snp rs28934583 20267475..20267475 "[omim:HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE]" http://www.snpedia.com/index.php?title=Rs28934583 reference = Chr16 snp rs28934584 20267817..20267817 "[omim:MEDULLARY CYSTIC KIDNEY DISEASE 2]" http://www.snpedia.com/index.php?title=Rs28934584 reference = Chr11 snp rs28934587 66055758..66055758 "[omim:BARDET-BIEDL SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28934587 reference = Chr19 snp rs28934588 53945626..53945626 "[omim:BOMBAY PHENOTYPE]" http://www.snpedia.com/index.php?title=Rs28934588 reference = Chr6 snp rs28934589 52219926..52219926 "[omim:CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934589 reference = Chr6 illumina rs28934590 32009632..32009632 "[omim:C2 DEFICIENCY, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934590 reference = Chr16 snp rs28934591 66027519..66027519 "[omim:APPARENT MINERALOCORTICOID EXCESS, HYPERTENSION DUE TO]" http://www.snpedia.com/index.php?title=Rs28934591 reference = Chr16 snp rs28934592 66027505..66027505 "[omim:APPARENT MINERALOCORTICOID EXCESS, HYPERTENSION DUE TO]" http://www.snpedia.com/index.php?title=Rs28934592 reference = Chr16 snp rs28934593 66028199..66028199 "[omim:APPARENT MINERALOCORTICOID EXCESS, HYPERTENSION DUE TO]" http://www.snpedia.com/index.php?title=Rs28934593 reference = Chr16 snp rs28934594 66028024..66028024 "[omim:APPARENT MINERALOCORTICOID EXCESS, HYPERTENSION DUE TO]" http://www.snpedia.com/index.php?title=Rs28934594 reference = Chr6 snp rs28934595 26199561..26199561 "[omim:PORPHYRIA VARIEGATA]" http://www.snpedia.com/index.php?title=Rs28934595 reference = Chr6 snp rs28934596 26199285..26199285 "[omim:HEMOCHROMATOSIS]" http://www.snpedia.com/index.php?title=Rs28934596 reference = Chr6 snp rs28934597 26199248..26199248 "[omim:HEMOCHROMATOSIS]" http://www.snpedia.com/index.php?title=Rs28934597 reference = Chr4 snp rs28934598 57155984..57155984 "[omim:GLYCINE ENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28934598 reference = Chr3 snp rs28934601 15661122..15661122 "[omim:BIOTINIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934601 reference = Chr21 snp rs28934602 37230968..37230968 "[omim:HOLOCARBOXYLASE SYNTHETASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934602 reference = Chr20 snp rs28934603 43953807..43953807 "[omim:GALACTOSIALIDOSIS]" http://www.snpedia.com/index.php?title=Rs28934603 reference = Chr12 snp rs28934604 56446123..56446123 "[omim:VITAMIN D-DEPENDENT RICKETS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28934604 reference = Chr12 snp rs28934605 56446069..56446069 "[omim:VITAMIN D-DEPENDENT RICKETS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28934605 reference = Chr12 snp rs28934606 56444560..56444560 "[omim:VITAMIN D-DEPENDENT RICKETS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28934606 reference = Chr12 snp rs28934607 56444219..56444219 "[omim:VITAMIN D-DEPENDENT RICKETS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28934607 reference = Chr4 snp rs28934608 187438481..187438481 "[omim:FACTOR XI DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934608 reference = Chr4 snp rs28934609 187446666..187446666 "[omim:FACTOR XI DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934609 reference = Chr11 snp rs28934610 76545598..76545598 "[omim:USHER SYNDROME, TYPE IB]" http://www.snpedia.com/index.php?title=Rs28934610 reference = ChrX snp rs28934611 10377535..10377535 "[omim:OPITZ SYNDROME, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28934611 reference = Chr3 snp rs28934868 24139617..24139617 "[omim:THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28934868 reference = Chr3 snp rs28934869 30708000..30708000 "[omim:MARFAN SYNDROME, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934869 reference = Chr19 snp rs28934870 60357227..60357227 "[omim:CARDIOMYOPATHY, FAMILIAL RESTRICTIVE]" http://www.snpedia.com/index.php?title=Rs28934870 reference = Chr19 snp rs28934871 60357326..60357326 "[omim:CARDIOMYOPATHY, FAMILIAL RESTRICTIVE]" http://www.snpedia.com/index.php?title=Rs28934871 reference = Chr16 snp rs28934872 2060573..2060573 "[omim:TUBEROUS SCLEROSIS 2]" http://www.snpedia.com/index.php?title=Rs28934872 reference = Chr17 snp rs28934873 7519257..7519257 "[omim:LI-FRAUMENI SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28934873 reference = Chr17 snp rs28934874 7519204..7519204 "[omim:BREAST CANCER]" http://www.snpedia.com/index.php?title=Rs28934874 reference = Chr17 snp rs28934875 7519243..7519243 "[omim:LI-FRAUMENI SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28934875 reference = Chr11 snp rs28934876 118476316..118476316 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij]" http://www.snpedia.com/index.php?title=Rs28934876 reference = Chr2 illumina rs28934877 234341718..234341718 "[omim:CRIGLER-NAJJAR SYNDROME, TYPE II]" http://www.snpedia.com/index.php?title=Rs28934877 reference = Chr20 snp rs28934878 3011745..3011745 "[omim:DIABETES INSIPIDUS, FAMILIAL CENTRAL]" http://www.snpedia.com/index.php?title=Rs28934878 reference = Chr12 snp rs28934879 6001387..6001387 "[omim:VON WILLEBRAND DISEASE, TYPE IIM]" http://www.snpedia.com/index.php?title=Rs28934879 reference = Chr1 snp rs28934880 119759594..119759594 "[omim:3-@BETA-HYDROXYSTEROID DEHYDROGENASE, TYPE II, DEFICIENCY OF]" http://www.snpedia.com/index.php?title=Rs28934880 reference = Chr3 snp rs28934881 184242169..184242169 "[omim:3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934881 reference = Chr3 snp rs28934882 184239583..184239583 "[omim:3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934882 reference = Chr5 snp rs28934883 70931255..70931255 "[omim:3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934883 reference = Chr5 snp rs28934884 70934204..70934204 "[omim:3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934884 reference = Chr3 snp rs28934885 33089133..33089133 "[omim:GM1-GANGLIOSIDOSIS, ADULT/CHRONIC TYPE]" http://www.snpedia.com/index.php?title=Rs28934885 reference = Chr3 snp rs28934886 33033314..33033314 "[omim:GM1-GANGLIOSIDOSIS, ADULT/CHRONIC TYPE]" http://www.snpedia.com/index.php?title=Rs28934886 reference = Chr3 snp rs28934887 137528771..137528771 "[omim:PROPIONIC ACIDEMIA]" http://www.snpedia.com/index.php?title=Rs28934887 reference = Chr6 snp rs28934888 26199164..26199164 "[omim:HEMOCHROMATOSIS]" http://www.snpedia.com/index.php?title=Rs28934888 reference = Chr6 snp rs28934889 26199128..26199128 "[omim:HFE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28934889 reference = Chr6 snp rs28934890 26199146..26199146 "[omim:HFE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28934890 reference = Chr21 snp rs28934891 43352041..43352041 "[omim:HOMOCYSTINURIA, PYRIDOXINE-RESPONSIVE]" http://www.snpedia.com/index.php?title=Rs28934891 reference = Chr21 snp rs28934892 43352106..43352106 "[omim:THROMBOSIS, HYPERHOMOCYSTEINEMIC]" http://www.snpedia.com/index.php?title=Rs28934892 reference = Chr1 snp rs28934894 23876237..23876237 "[omim:HMG-CoA LYASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934894 reference = Chr6 snp rs28934895 80935381..80935381 "[omim:MAPLE SYRUP URINE DISEASE, CLASSIC, TYPE IB]" http://www.snpedia.com/index.php?title=Rs28934895 reference = Chr12 snp rs28934896 108495569..108495569 "[omim:MEVALONIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28934896 reference = Chr12 snp rs28934897 108497040..108497040 "[omim:HYPER-IgD SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934897 reference = Chr12 snp rs28934898 101736738..101736738 "[omim:PHENYLKETONURIA]" http://www.snpedia.com/index.php?title=Rs28934898 reference = Chr12 snp rs28934899 101736722..101736722 "[omim:PHENYLKETONURIA]" http://www.snpedia.com/index.php?title=Rs28934899 reference = Chr12 snp rs28934900 101749126..101749126 "[omim:PHENYLKETONURIA]" http://www.snpedia.com/index.php?title=Rs28934900 reference = Chr4 snp rs28934901 187580548..187580548 "[omim:FACTOR XI DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28934901 reference = Chr7 snp rs28934902 141945948..141945948 "[omim:PANCREATITIS, HEREDITARY]" http://www.snpedia.com/index.php?title=Rs28934902 reference = Chr11 snp rs28934903 76550843..76550843 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 11]" http://www.snpedia.com/index.php?title=Rs28934903 reference = ChrX snp rs28934904 152950076..152950076 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934904 reference = ChrX snp rs28934905 152950009..152950009 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934905 reference = ChrX snp rs28934906 152950000..152950000 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934906 reference = ChrX snp rs28934907 152950913..152950913 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28934907 reference = ChrX snp rs28934908 152950054..152950054 "[omim:MENTAL RETARDATION, X-LINKED 16]" http://www.snpedia.com/index.php?title=Rs28934908 reference = ChrX snp rs28935168 152950931..152950931 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935168 reference = ChrX snp rs28935169 153252563..153252563 "[omim:HETEROTOPIA, PERIVENTRICULAR]" http://www.snpedia.com/index.php?title=Rs28935169 reference = ChrX snp rs28935170 67976299..67976299 "[omim:CRANIOFRONTONASAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935170 reference = ChrX snp rs28935171 20083474..20083474 "[omim:COFFIN-LOWRY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935171 reference = ChrX illumina rs28935172 110530992..110530992 "[omim:LISSENCEPHALY, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935172 reference = ChrX snp rs28935173 153565131..153565131 "[omim:DYSKERATOSIS CONGENITA, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935173 reference = ChrX illumina rs28935174 48270588..48270588 "[omim:CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT]" http://www.snpedia.com/index.php?title=Rs28935174 reference = ChrX snp rs28935175 151705000..151705000 "[omim:CHILD SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935175 reference = ChrX snp rs28935176 100495579..100495579 "[omim:AGAMMAGLOBULINEMIA, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935176 reference = ChrX snp rs28935177 79169015..79169015 "[omim:CLEFT PALATE WITH ANKYLOGLOSSIA]" http://www.snpedia.com/index.php?title=Rs28935177 reference = ChrX snp rs28935178 48298962..48298962 "[omim:THROMBOCYTOPENIA, X-LINKED, INTERMITTENT]" http://www.snpedia.com/index.php?title=Rs28935178 reference = ChrX snp rs28935179 133237301..133237301 "[omim:BORJESON-FORSSMAN-LEHMANN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935179 reference = ChrX snp rs28935180 30085992..30085992 "[omim:ADRENAL HYPOPLASIA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28935180 reference = ChrX snp rs28935181 37425074..37425074 "[omim:GRANULOMATOUS DISEASE, CHRONIC, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935181 reference = ChrX snp rs28935182 37419356..37419356 "[omim:GRANULOMATOUS DISEASE, CHRONIC, X-LINKED, VARIANT]" http://www.snpedia.com/index.php?title=Rs28935182 reference = ChrX snp rs28935183 39690569..39690569 "[omim:MICROPHTHALMIA, SYNDROMIC 2]" http://www.snpedia.com/index.php?title=Rs28935183 reference = ChrX snp rs28935184 123229661..123229661 "[omim:LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1]" http://www.snpedia.com/index.php?title=Rs28935184 reference = ChrX snp rs28935185 9521413..9521413 "[omim:ALBINISM, OCULAR, TYPE I]" http://www.snpedia.com/index.php?title=Rs28935185 reference = Chr4 snp rs28935186 96981042..96981042 "[omim:PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935186 reference = Chr4 snp rs28935187 96981261..96981261 "[omim:PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935187 reference = ChrX snp rs28935188 19283432..19283432 "[omim:PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935188 reference = ChrX snp rs28935189 54918696..54918696 "[omim:ANEMIA, HEREDITARY SIDEROBLASTIC]" http://www.snpedia.com/index.php?title=Rs28935189 reference = ChrX snp rs28935190 54930669..54930669 "[omim:ANEMIA, HEREDITARY SIDEROBLASTIC]" http://www.snpedia.com/index.php?title=Rs28935190 reference = ChrX snp rs28935199 152982272..152982272 "Colorblindness is typically caused by rearrangements in the region of the X chromosome harboring the..." http://www.snpedia.com/index.php?title=Rs28935199 reference = ChrX snp rs28935200 152945166..152945166 "[omim:COLORBLINDNESS, PROTAN]" http://www.snpedia.com/index.php?title=Rs28935200 reference = ChrX snp rs28935201 153653737..153653737 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935201 reference = ChrX snp rs28935202 153810137..153810137 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935202 reference = ChrX snp rs28935203 153810163..153810163 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935203 reference = ChrX snp rs28935204 153789065..153789065 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935204 reference = ChrX snp rs28935205 153789044..153789044 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935205 reference = ChrX snp rs28935206 153789029..153789029 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935206 reference = ChrX snp rs28935207 153789017..153789017 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935207 reference = ChrX snp rs28935208 153788990..153788990 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935208 reference = ChrX snp rs28935209 153785120..153785120 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935209 reference = ChrX snp rs28935211 153785112..153785112 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935211 reference = ChrX snp rs28935212 153785025..153785025 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935212 reference = ChrX snp rs28935213 153785023..153785023 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935213 reference = ChrX snp rs28935214 153761438..153761438 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935214 reference = ChrX snp rs28935215 153761423..153761423 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935215 reference = ChrX snp rs28935216 153761417..153761417 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28935216 reference = ChrX illumina rs28935468 152949557..152949557 "[omim:RETT SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935468 reference = ChrX snp rs28935469 153249406..153249406 "[omim:OTOPALATODIGITAL SYNDROME, TYPE I]" http://www.snpedia.com/index.php?title=Rs28935469 reference = ChrX snp rs28935470 153249067..153249067 "[omim:OTOPALATODIGITAL SYNDROME, TYPE II]" http://www.snpedia.com/index.php?title=Rs28935470 reference = ChrX snp rs28935471 153241881..153241881 "[omim:FRONTOMETAPHYSEAL DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28935471 reference = ChrX snp rs28935472 153241795..153241795 "[omim:MELNICK-NEEDLES SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935472 reference = ChrX snp rs28935473 153241761..153241761 "[omim:MELNICK-NEEDLES SYNDROME]" http://www.snpedia.com/index.php?title=Rs28935473 reference = ChrX snp rs28935474 2862911..2862911 "[omim:CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28935474 reference = ChrX illumina rs28935475 53475759..53475759 "[omim:2-@METHYL-3-HYDROXYBUTYRYL-CoA DEHYDROGENASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935475 reference = ChrX snp rs28935476 53475783..53475783 "[omim:2-@METHYL-3-HYDROXYBUTYRYL-CoA DEHYDROGENASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935476 reference = ChrX illumina rs28935477 48994846..48994846 "[omim:IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935477 reference = ChrX snp rs28935478 100499974..100499974 "[omim:HYPOAGAMMAGLOBULINEMIA, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935478 reference = ChrX snp rs28935479 24941177..24941177 "[omim:MENTAL RETARDATION, X-LINKED 54]" http://www.snpedia.com/index.php?title=Rs28935479 reference = ChrX illumina rs28935480 47371163..47371163 "[omim:PROPERDIN DEFICIENCY, TYPE I]" http://www.snpedia.com/index.php?title=Rs28935480 reference = ChrX snp rs28935481 30232711..30232711 "[omim:ADRENAL HYPOPLASIA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28935481 reference = ChrX snp rs28935482 30236529..30236529 "[omim:ADRENAL HYPOPLASIA, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28935482 reference = ChrX snp rs28935483 100920663..100920663 "[omim:GLYCEROL KINASE DEFICIENCY, ISOLATED]" http://www.snpedia.com/index.php?title=Rs28935483 reference = ChrX snp rs28935484 55064279..55064279 "[omim:ANEMIA, HEREDITARY SIDEROBLASTIC, PYRIDOXINE REFRACTORY]" http://www.snpedia.com/index.php?title=Rs28935484 reference = ChrX snp rs28935496 152824491..152824491 "[omim:DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28935496 reference = ChrX snp rs28935499 153847994..153847994 "[omim:FACTOR VIII (OKAYAMA)]" http://www.snpedia.com/index.php?title=Rs28935499 reference = Chr5 snp rs28935768 147191332..147191332 "[omim:PANCREATITIS, CHRONIC]" http://www.snpedia.com/index.php?title=Rs28935768 reference = Chr3 snp rs28935769 58391618..58391618 "[omim:PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28935769 reference = Chr6 snp rs28935770 54743514..54743514 "[omim:BLADDER CANCER, TRANSITIONAL CELL, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28935770 reference = ChrX snp rs28936068 77072858..77072858 "[omim:CUTIS LAXA, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28936068 reference = ChrX snp rs28936069 67976276..67976276 "[omim:CRANIOFRONTONASAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936069 reference = ChrX snp rs28936070 67976277..67976277 "[omim:CRANIOFRONTONASAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936070 reference = ChrX snp rs28936071 67976297..67976297 "[omim:CRANIOFRONTONASAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936071 reference = ChrX illumina rs28936072 153646941..153646941 "[omim:HOYERAAL-HREIDARSSON SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936072 reference = ChrX snp rs28936073 48138651..48138651 "[omim:CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT]" http://www.snpedia.com/index.php?title=Rs28936073 reference = ChrX snp rs28936074 24790711..24790711 "[omim:MYOCLONIC EPILEPSY, X-LINKED, WITH MENTAL RETARDATION AND SPASTICITY]" http://www.snpedia.com/index.php?title=Rs28936074 reference = ChrX snp rs28936075 24790774..24790774 "[omim:LISSENCEPHALY, X-LINKED, WITH AMBIGUOUS GENITALIA]" http://www.snpedia.com/index.php?title=Rs28936075 reference = ChrX snp rs28936076 24790741..24790741 "[omim:LISSENCEPHALY, X-LINKED, WITH AMBIGUOUS GENITALIA]" http://www.snpedia.com/index.php?title=Rs28936076 reference = ChrX snp rs28936077 24793414..24793414 "[omim:MENTAL RETARDATION, X-LINKED 54]" http://www.snpedia.com/index.php?title=Rs28936077 reference = ChrX snp rs28936078 24790771..24790771 "[omim:CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA]" http://www.snpedia.com/index.php?title=Rs28936078 reference = ChrX snp rs28936079 48302970..48302970 "[omim:NEUTROPENIA, SEVERE CONGENITAL, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28936079 reference = ChrX snp rs28936080 102850435..102850435 "[omim:PELIZAEUS-MERZBACHER DISEASE, CONNATAL]" http://www.snpedia.com/index.php?title=Rs28936080 reference = ChrX snp rs28936081 19133488..19133488 "[omim:LEIGH SYNDROME, X-LINKED]" http://www.snpedia.com/index.php?title=Rs28936081 reference = ChrX snp rs28936083 153789012..153789012 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28936083 reference = Chr19 illumina rs28936368 18754939..18754939 "[omim:EPIPHYSEAL DYSPLASIA, MULTIPLE, FAIRBANK TYPE]" http://www.snpedia.com/index.php?title=Rs28936368 reference = Chr8 snp rs28936369 64139407..64139407 "[omim:ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28936369 reference = Chr11 snp rs28936370 17375103..17375103 "[omim:HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1]" http://www.snpedia.com/index.php?title=Rs28936370 reference = Chr11 illumina rs28936371 17372457..17372457 "[omim:HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1]" http://www.snpedia.com/index.php?title=Rs28936371 reference = Chr11 snp rs28936372 68308943..68308943 "[omim:CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28936372 reference = Chr11 snp rs28936373 68305926..68305926 "[omim:CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28936373 reference = Chr11 snp rs28936374 68284285..68284285 "[omim:CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28936374 reference = Chr1 snp rs28936375 53374785..53374785 "[omim:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET]" http://www.snpedia.com/index.php?title=Rs28936375 reference = Chr1 snp rs28936376 53390968..53390968 "[omim:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET]" http://www.snpedia.com/index.php?title=Rs28936376 reference = Chr2 snp rs28936377 219750397..219750397 "[omim:BRACHYDACTYLY, TYPE A1]" http://www.snpedia.com/index.php?title=Rs28936377 reference = Chr2 snp rs28936378 219750414..219750414 "[omim:BRACHYDACTYLY, TYPE A1]" http://www.snpedia.com/index.php?title=Rs28936378 reference = Chr1 snp rs28936379 225143301..225143301 "[omim:ALZHEIMER DISEASE, FAMILIAL, 4]" http://www.snpedia.com/index.php?title=Rs28936379 reference = Chr1 snp rs28936380 223379982..223379982 "[omim:ALZHEIMER DISEASE, FAMILIAL, 4]" http://www.snpedia.com/index.php?title=Rs28936380 reference = Chr1 snp rs28936381 92653731..92653731 "[omim:NEUTROPENIA, CONGENITAL, AUTOSOMAL DOMINANT 2]" http://www.snpedia.com/index.php?title=Rs28936381 reference = Chr1 snp rs28936382 92714235..92714235 "[omim:NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS]" http://www.snpedia.com/index.php?title=Rs28936382 reference = Chr4 snp rs28936383 52589822..52589822 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E]" http://www.snpedia.com/index.php?title=Rs28936383 reference = Chr4 snp rs28936384 52736929..52736929 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E]" http://www.snpedia.com/index.php?title=Rs28936384 reference = Chr4 snp rs28936385 52736881..52736881 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E]" http://www.snpedia.com/index.php?title=Rs28936385 reference = Chr4 snp rs28936386 52736902..52736902 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E]" http://www.snpedia.com/index.php?title=Rs28936386 reference = Chr16 snp rs28936387 55470566..55470566 "[omim:GITELMAN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936387 reference = Chr16 snp rs28936388 55461532..55461532 "[omim:GITELMAN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936388 reference = Chr16 snp rs28936389 55476741..55476741 "[omim:GITELMAN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936389 reference = Chr6 snp rs28936390 76607115..76607115 "[omim:DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 37]" http://www.snpedia.com/index.php?title=Rs28936390 reference = Chr6 snp rs28936391 76607736..76607736 "[omim:DEAFNESS, SENSORINEURAL, WITH HYPERTROPHIC CARDIOMYOPATHY]" http://www.snpedia.com/index.php?title=Rs28936391 reference = Chr18 snp rs28936392 46858653..46858653 "[omim:PANCREATIC CARCINOMA]" http://www.snpedia.com/index.php?title=Rs28936392 reference = Chr18 snp rs28936393 46847404..46847404 "[omim:JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936393 reference = Chr18 snp rs28936394 46845889..46845889 "[omim:JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936394 reference = Chr1 snp rs28936395 23105933..23105933 "[omim:PROSTATE CANCER, PROGRESSION AND METASTASIS OF]" http://www.snpedia.com/index.php?title=Rs28936395 reference = Chr20 snp rs28936396 32994070..32994070 "[omim:GLUTATHIONE SYNTHETASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28936396 reference = Chr20 snp rs28936397 33488606..33488606 "[omim:BRACHYDACTYLY, TYPE C]" http://www.snpedia.com/index.php?title=Rs28936397 reference = Chr12 snp rs28936398 50596270..50596270 "[omim:TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE II]" http://www.snpedia.com/index.php?title=Rs28936398 reference = Chr12 snp rs28936399 50596165..50596165 "[omim:TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28936399 reference = Chr12 snp rs28936400 50596231..50596231 "[omim:TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28936400 reference = Chr12 snp rs28936401 50596158..50596158 "[omim:TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28936401 reference = Chr12 snp rs28936402 50596234..50596234 "[omim:PULMONARY ARTERIAL HYPERTENSION, HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED]" http://www.snpedia.com/index.php?title=Rs28936402 reference = Chr9 snp rs28936403 97281144..97281144 "[omim:HOLOPROSENCEPHALY 7]" http://www.snpedia.com/index.php?title=Rs28936403 reference = Chr9 snp rs28936404 95310655..95310655 "[omim:HOLOPROSENCEPHALY 7]" http://www.snpedia.com/index.php?title=Rs28936404 reference = Chr9 snp rs28936405 95299863..95299863 "[omim:HOLOPROSENCEPHALY 7]" http://www.snpedia.com/index.php?title=Rs28936405 reference = Chr2 snp rs28936406 74085670..74085670 "[omim:MITOCHONDRIAL DNA-DEPLETION SYNDROME, HEPATOCEREBRAL FORM]" http://www.snpedia.com/index.php?title=Rs28936406 reference = Chr3 snp rs28936407 12433330..12433330 "[omim:COLON CANCER, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28936407 reference = Chr4 snp rs28936408 111762905..111762905 "[omim:RIEGER SYNDROME, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28936408 reference = Chr4 snp rs28936409 111761908..111761908 "[omim:RIEGER SYNDROME, TYPE 1]" http://www.snpedia.com/index.php?title=Rs28936409 reference = Chr2 snp rs28936410 111858280..111858280 "[omim:LISSENCEPHALY SEQUENCE, ISOLATED]" http://www.snpedia.com/index.php?title=Rs28936410 reference = Chr2 snp rs28936411 111858528..111858528 "[omim:SUBCORTICAL LAMINAR HETEROTOPIA]" http://www.snpedia.com/index.php?title=Rs28936411 reference = Chr16 snp rs28936412 2316029..2316029 "[omim:SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3]" http://www.snpedia.com/index.php?title=Rs28936412 reference = Chr2 snp rs28936413 38210028..38210028 "[omim:GLAUCOMA 3, PRIMARY CONGENITAL, A]" http://www.snpedia.com/index.php?title=Rs28936413 reference = Chr2 snp rs28936414 38210045..38210045 "[omim:GLAUCOMA, EARLY-ONSET, DIGENIC]" http://www.snpedia.com/index.php?title=Rs28936414 reference = ChrNone snp rs28936415 10627089..10627089 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia]" http://www.snpedia.com/index.php?title=Rs28936415 reference = Chr3 snp rs28936416 57208910..57208910 "[omim:PITUITARY HORMONE DEFICIENCY, COMBINED, HESX1-RELATED]" http://www.snpedia.com/index.php?title=Rs28936416 reference = Chr19 snp rs28936668 18757906..18757906 "[omim:EPIPHYSEAL DYSPLASIA, MULTIPLE, FAIRBANK TYPE]" http://www.snpedia.com/index.php?title=Rs28936668 reference = Chr19 snp rs28936669 18757846..18757846 "[omim:PSEUDOACHONDROAPLASIA]" http://www.snpedia.com/index.php?title=Rs28936669 reference = Chr5 snp rs28936670 172594620..172594620 "[omim:TETRALOGY OF FALLOT]" http://www.snpedia.com/index.php?title=Rs28936670 reference = Chr14 snp rs28936671 36056713..36056713 "[omim:CHOREA, BENIGN HEREDITARY]" http://www.snpedia.com/index.php?title=Rs28936671 reference = Chr14 snp rs28936672 36056727..36056727 "[omim:CHOREA, BENIGN HEREDITARY]" http://www.snpedia.com/index.php?title=Rs28936672 reference = Chr1 snp rs28936673 53451761..53451761 "[omim:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE]" http://www.snpedia.com/index.php?title=Rs28936673 reference = Chr1 snp rs28936674 53448454..53448454 "[omim:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE]" http://www.snpedia.com/index.php?title=Rs28936674 reference = Chr7 snp rs28936675 155297487..155297487 "[omim:HOLOPROSENCEPHALY 3]" http://www.snpedia.com/index.php?title=Rs28936675 reference = Chr1 illumina rs28936676 159406881..159406881 "[omim:VARIEGATE PORPHYRIA, HOMOZYGOUS]" http://www.snpedia.com/index.php?title=Rs28936676 reference = Chr1 snp rs28936677 159403296..159403296 "[omim:VARIEGATE PORPHYRIA, HOMOZYGOUS]" http://www.snpedia.com/index.php?title=Rs28936677 reference = Chr11 snp rs28936678 17365775..17365775 "[omim:HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28936678 reference = Chr17 snp rs28936679 71977408..71977408 "[omim:DELAYED SLEEP PHASE SYNDROME, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs28936679 reference = Chr1 snp rs28936680 152827768..152827768 "[omim:DYSCHROMATOSIS SYMMETRICA HEREDITARIA]" http://www.snpedia.com/index.php?title=Rs28936680 reference = Chr1 snp rs28936681 152824093..152824093 "[omim:DYSCHROMATOSIS SYMMETRICA HEREDITARIA]" http://www.snpedia.com/index.php?title=Rs28936681 reference = Chr17 snp rs28936682 15074973..15074973 "[omim:DEJERINE-SOTTAS SYNDROME, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28936682 reference = Chr20 snp rs28936683 33485305..33485305 "[omim:FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY]" http://www.snpedia.com/index.php?title=Rs28936683 reference = Chr3 snp rs28936684 123463252..123463252 "[omim:HYPERPARATHYROIDISM, NEONATAL SEVERE PRIMARY]" http://www.snpedia.com/index.php?title=Rs28936684 reference = Chr3 snp rs28936685 8762357..8762357 "[omim:RIPPLING MUSCLE DISEASE 2]" http://www.snpedia.com/index.php?title=Rs28936685 reference = Chr3 snp rs28936686 8762374..8762374 "[omim:RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28936686 reference = Chr12 snp rs28936687 50594496..50594496 "[omim:PULMONARY ARTERIAL HYPERTENSION, HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED]" http://www.snpedia.com/index.php?title=Rs28936687 reference = Chr12 snp rs28936688 50595534..50595534 "[omim:TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28936688 reference = Chr2 snp rs28936689 87646741..87646741 "[omim:LISSENCEPHALY SEQUENCE, ISOLATED]" http://www.snpedia.com/index.php?title=Rs28936689 reference = Chr16 snp rs28936690 2268353..2268353 "[omim:SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3]" http://www.snpedia.com/index.php?title=Rs28936690 reference = Chr16 snp rs28936691 2268018..2268018 "[omim:SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3]" http://www.snpedia.com/index.php?title=Rs28936691 reference = Chr20 snp rs28936692 62151004..62151004 "[omim:HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936692 reference = Chr20 snp rs28936693 62151031..62151031 "[omim:HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936693 reference = Chr1 snp rs28936694 169872007..169872007 "[omim:GLAUCOMA 1, OPEN ANGLE, A, DIGENIC]" http://www.snpedia.com/index.php?title=Rs28936694 reference = Chr17 snp rs28936695 36276579..36276579 "[omim:MEESMANN CORNEAL DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28936695 reference = Chr17 snp rs28936696 56915613..56915613 "[omim:SMALL PATELLA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28936696 reference = Chr17 snp rs28936697 30927035..30927035 "[omim:PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 3]" http://www.snpedia.com/index.php?title=Rs28936697 reference = Chr17 snp rs28936698 30928577..30928577 "[omim:PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 3]" http://www.snpedia.com/index.php?title=Rs28936698 reference = Chr2 snp rs28936699 201782356..201782356 "[omim:NON-HODGKIN LYMPHOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28936699 reference = Chr2 snp rs28936700 38155854..38155854 "[omim:GLAUCOMA 3, PRIMARY CONGENITAL, A]" http://www.snpedia.com/index.php?title=Rs28936700 reference = Chr2 illumina rs28936701 38151596..38151596 "[omim:GLAUCOMA 3, PRIMARY CONGENITAL, A]" http://www.snpedia.com/index.php?title=Rs28936701 reference = Chr3 snp rs28936703 57207314..57207314 "[omim:SEPTOOPTIC DYSPLASIA, MILD]" http://www.snpedia.com/index.php?title=Rs28936703 reference = Chr3 snp rs28936704 57207282..57207282 "[omim:GROWTH HORMONE DEFICIENCY, HESX1-RELATED]" http://www.snpedia.com/index.php?title=Rs28936704 reference = ChrX snp rs28936968 153753110..153753110 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28936968 reference = ChrX snp rs28936969 153753099..153753099 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28936969 reference = ChrX snp rs28936970 153655104..153655104 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28936970 reference = Chr3 snp rs28936971 38576665..38576665 "[omim:SICK SINUS SYNDROME, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28936971 reference = Chr7 snp rs28936972 30412852..30412852 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D]" http://www.snpedia.com/index.php?title=Rs28936972 reference = ChrX snp rs28937268 153761396..153761396 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937268 reference = ChrX snp rs28937269 153761379..153761379 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937269 reference = ChrX snp rs28937270 153761339..153761339 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937270 reference = ChrX snp rs28937271 153761333..153761333 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937271 reference = ChrX snp rs28937272 153847551..153847551 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937272 reference = ChrX snp rs28937273 153847534..153847534 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937273 reference = ChrX snp rs28937274 153753117..153753117 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937274 reference = ChrX snp rs28937275 153753116..153753116 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937275 reference = ChrX snp rs28937276 153749058..153749058 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937276 reference = ChrX snp rs28937277 153749052..153749052 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937277 reference = ChrX snp rs28937278 153749040..153749040 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937278 reference = ChrX snp rs28937279 153749039..153749039 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937279 reference = ChrX snp rs28937280 153749028..153749028 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937280 reference = ChrX snp rs28937281 153749006..153749006 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937281 reference = ChrX snp rs28937282 153748958..153748958 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937282 reference = ChrX snp rs28937283 153748959..153748959 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937283 reference = ChrX snp rs28937284 153745966..153745966 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937284 reference = ChrX snp rs28937285 153813044..153813044 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937285 reference = ChrX snp rs28937286 153810136..153810136 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937286 reference = ChrX snp rs28937287 153698449..153698449 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937287 reference = ChrX snp rs28937288 153698447..153698447 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937288 reference = ChrX snp rs28937289 153698436..153698436 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937289 reference = ChrX snp rs28937290 153696977..153696977 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937290 reference = ChrX snp rs28937291 153696978..153696978 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937291 reference = ChrX snp rs28937292 153696968..153696968 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937292 reference = ChrX snp rs28937293 153696954..153696954 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937293 reference = ChrX snp rs28937294 153785494..153785494 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937294 reference = ChrX snp rs28937295 153785473..153785473 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937295 reference = ChrX snp rs28937296 153695947..153695947 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937296 reference = ChrX snp rs28937297 153695945..153695945 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937297 reference = ChrX snp rs28937298 153694099..153694099 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937298 reference = ChrX snp rs28937299 153691925..153691925 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937299 reference = ChrX snp rs28937300 153691855..153691855 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937300 reference = ChrX snp rs28937301 153688207..153688207 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937301 reference = ChrX snp rs28937302 153655103..153655103 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937302 reference = ChrX snp rs28937303 153655091..153655091 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937303 reference = ChrX snp rs28937304 153655092..153655092 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937304 reference = ChrX snp rs28937305 153653789..153653789 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937305 reference = ChrX snp rs28937306 153653738..153653738 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937306 reference = ChrX snp rs28937307 153652567..153652567 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937307 reference = ChrX snp rs28937308 153652517..153652517 "[omim:HEMOPHILIA A]" http://www.snpedia.com/index.php?title=Rs28937308 reference = ChrX snp rs28937309 8314629..8314629 "[omim:KALLMANN SYNDROME 1]" http://www.snpedia.com/index.php?title=Rs28937309 reference = ChrX snp rs28937310 148270425..148270425 "[omim:MUCOPOLYSACCHARIDOSIS TYPE II]" http://www.snpedia.com/index.php?title=Rs28937310 reference = ChrX snp rs28937311 148290615..148290615 "[omim:MUCOPOLYSACCHARIDOSIS TYPE II]" http://www.snpedia.com/index.php?title=Rs28937311 reference = ChrX snp rs28937312 105165915..105165915 "[omim:THYROXINE-BINDING GLOBULIN DEFICIENCY, COMPLETE]" http://www.snpedia.com/index.php?title=Rs28937312 reference = Chr9 snp rs28937313 106624622..106624622 "[omim:TANGIER DISEASE]" http://www.snpedia.com/index.php?title=Rs28937313 reference = Chr9 snp rs28937314 106624623..106624623 "[omim:TANGIER DISEASE]" http://www.snpedia.com/index.php?title=Rs28937314 reference = Chr16 snp rs28937315 3747896..3747896 "[omim:RUBINSTEIN-TAYBI SYNDROME, INCOMPLETE]" http://www.snpedia.com/index.php?title=Rs28937315 reference = Chr3 snp rs28937316 38567936..38567936 "[omim:LONG QT SYNDROME 3]" http://www.snpedia.com/index.php?title=Rs28937316 reference = Chr3 snp rs28937317 38576913..38576913 "[omim:LONG QT SYNDROME 3]" http://www.snpedia.com/index.php?title=Rs28937317 reference = Chr3 snp rs28937318 38623204..38623204 "[omim:BRUGADA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937318 reference = Chr3 snp rs28937319 38578980..38578980 "[omim:SICK SINUS SYNDROME, CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28937319 reference = Chr1 snp rs28937320 120019236..120019236 "[omim:HMG-CoA SYNTHASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28937320 reference = Chr19 snp rs28937321 15164315..15164315 "[omim:CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28937321 reference = Chr7 snp rs28937322 30422585..30422585 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D]" http://www.snpedia.com/index.php?title=Rs28937322 reference = Chr7 snp rs28937323 30441454..30441454 "[omim:NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V]" http://www.snpedia.com/index.php?title=Rs28937323 reference = Chr7 snp rs28937568 75771260..75771260 "[omim:NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB]" http://www.snpedia.com/index.php?title=Rs28937568 reference = Chr7 snp rs28937569 75771353..75771353 "[omim:NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB]" http://www.snpedia.com/index.php?title=Rs28937569 reference = Chr11 snp rs28937571 87666979..87666979 "[omim:PERIODONTITIS, AGGRESSIVE, 1]" http://www.snpedia.com/index.php?title=Rs28937571 reference = Chr16 snp rs28937572 65757228..65757228 "[omim:CATARACT, LAMELLAR]" http://www.snpedia.com/index.php?title=Rs28937572 reference = Chr16 snp rs28937573 65757245..65757245 "[omim:CATARACT, MARNER TYPE]" http://www.snpedia.com/index.php?title=Rs28937573 reference = Chr9 snp rs28937575 99656187..99656187 "[omim:HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE]" http://www.snpedia.com/index.php?title=Rs28937575 reference = ChrNone snp rs28937576 25493688..25493688 "[omim:SDHD POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28937576 reference = ChrNone snp rs28937577 25493573..25493573 "[omim:CARCINOID TUMORS, INTESTINAL]" http://www.snpedia.com/index.php?title=Rs28937577 reference = Chr22 snp rs28937578 39904323..39904323 "[omim:COLORECTAL CANCER]" http://www.snpedia.com/index.php?title=Rs28937578 reference = Chr9 snp rs28937579 103173282..103173282 "[omim:HYPERCHOLANEMIA, FAMILIAL]" http://www.snpedia.com/index.php?title=Rs28937579 reference = Chr17 snp rs28937580 52026686..52026686 "[omim:SYMPHALANGISM, PROXIMAL]" http://www.snpedia.com/index.php?title=Rs28937580 reference = Chr2 snp rs28937581 71650938..71650938 "[omim:MIYOSHI MYOPATHY]" http://www.snpedia.com/index.php?title=Rs28937581 reference = Chr3 snp rs28937582 162286440..162286440 "[omim:BLOOD GROUP--P SYSTEM, P(k) ANTIGEN]" http://www.snpedia.com/index.php?title=Rs28937582 reference = Chr1 snp rs28937583 35023051..35023051 "[omim:ERYTHROKERATODERMIA VARIABILIS, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28937583 reference = Chr14 snp rs28937584 80680052..80680052 "[omim:THYROID CARCINOMA WITH THYROTOXICOSIS]" http://www.snpedia.com/index.php?title=Rs28937584 reference = Chr12 snp rs28937585 50581089..50581089 "[omim:LARSEN SYNDROME, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937585 reference = Chr12 snp rs28937586 50581125..50581125 "[omim:ATELOSTEOGENESIS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28937586 reference = Chr3 snp rs28937587 58070394..58070394 "[omim:ATELOSTEOGENESIS, TYPE III]" http://www.snpedia.com/index.php?title=Rs28937587 reference = Chr1 snp rs28937588 41058152..41058152 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2]" http://www.snpedia.com/index.php?title=Rs28937588 reference = Chr1 snp rs28937589 41057721..41057721 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2]" http://www.snpedia.com/index.php?title=Rs28937589 reference = Chr2 snp rs28937590 219234186..219234186 "[omim:GRACILE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937590 reference = Chr2 snp rs28937591 26538128..26538128 "[omim:DEAFNESS, AUTOSOMAL RECESSIVE 9]" http://www.snpedia.com/index.php?title=Rs28937591 reference = Chr5 snp rs28937592 121814302..121814302 "[omim:PARKINSON DISEASE]" http://www.snpedia.com/index.php?title=Rs28937592 reference = Chr10 snp rs28937593 73437706..73437706 "[omim:SPONDYLOEPIPHYSEAL DYSPLASIA, OMANI TYPE]" http://www.snpedia.com/index.php?title=Rs28937593 reference = Chr9 snp rs28937594 36207396..36207396 "[omim:INCLUSION BODY MYOPATHY, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28937594 reference = Chr1 snp rs28937595 167713309..167713309 "[omim:THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937595 reference = Chr3 snp rs28937596 185344593..185344593 "[omim:LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER]" http://www.snpedia.com/index.php?title=Rs28937596 reference = Chr5 snp rs28937597 137234409..137234409 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A]" http://www.snpedia.com/index.php?title=Rs28937597 reference = Chr22 snp rs28937598 49309196..49309196 "[omim:CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28937598 reference = Chr22 snp rs28937868 49309309..49309309 "[omim:CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28937868 reference = Chr5 snp rs28937869 176968601..176968601 "[omim:EHLERS-DANLOS SYNDROME, PROGEROID FORM]" http://www.snpedia.com/index.php?title=Rs28937869 reference = Chr14 snp rs28937870 74586042..74586042 "[omim:COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7]" http://www.snpedia.com/index.php?title=Rs28937870 reference = Chr14 snp rs28937871 74584616..74584616 "[omim:COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7]" http://www.snpedia.com/index.php?title=Rs28937871 reference = Chr13 snp rs28937872 19695357..19695357 "[omim:ECTODERMAL DYSPLASIA, HIDROTIC]" http://www.snpedia.com/index.php?title=Rs28937872 reference = Chr15 snp rs28937873 69892967..69892967 "[omim:ENHANCED S-CONE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937873 reference = Chr10 snp rs28937874 95547024..95547024 "[omim:EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937874 reference = Chr20 snp rs28937875 10342008..10342008 "[omim:BARDET-BIEDL SYNDROME 6]" http://www.snpedia.com/index.php?title=Rs28937875 reference = Chr6 snp rs28937876 41234707..41234707 "[omim:POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28937876 reference = Chr16 snp rs28937877 74070707..74070707 "[omim:MACULAR CORNEAL DYSTROPHY, TYPE I]" http://www.snpedia.com/index.php?title=Rs28937877 reference = Chr16 snp rs28937878 74070619..74070619 "[omim:MACULAR CORNEAL DYSTROPHY, TYPE I]" http://www.snpedia.com/index.php?title=Rs28937878 reference = Chr16 snp rs28937879 74070629..74070629 "[omim:MACULAR CORNEAL DYSTROPHY, TYPE I]" http://www.snpedia.com/index.php?title=Rs28937879 reference = Chr20 snp rs28937880 47003521..47003521 "[omim:PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28937880 reference = Chr12 snp rs28937881 4350002..4350002 "[omim:HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937881 reference = Chr12 snp rs28937882 4349991..4349991 "[omim:HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937882 reference = Chr14 snp rs28937883 20863942..20863942 "[omim:CONE-ROD DYSTROPHY 9]" http://www.snpedia.com/index.php?title=Rs28937883 reference = Chr3 snp rs28937884 140148004..140148004 "[omim:BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28937884 reference = Chr3 snp rs28937885 140147483..140147483 "[omim:PREMATURE OVARIAN FAILURE 3]" http://www.snpedia.com/index.php?title=Rs28937885 reference = Chr11 snp rs28937886 45789290..45789290 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc]" http://www.snpedia.com/index.php?title=Rs28937886 reference = Chr10 illumina rs28937887 102738958..102738958 "[omim:PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, DIGENIC]" http://www.snpedia.com/index.php?title=Rs28937887 reference = Chr8 snp rs28937888 143819619..143819619 "[omim:MAL DE MELEDA]" http://www.snpedia.com/index.php?title=Rs28937888 reference = Chr8 snp rs28937889 143820805..143820805 "[omim:MAL DE MELEDA]" http://www.snpedia.com/index.php?title=Rs28937889 reference = Chr4 snp rs28937890 6354594..6354594 "[omim:WOLFRAM SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937890 reference = Chr4 snp rs28937891 6354507..6354507 "[omim:WOLFRAM SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937891 reference = Chr4 snp rs28937892 6353934..6353934 "[omim:WOLFRAM SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937892 reference = Chr4 snp rs28937893 6354569..6354569 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6]" http://www.snpedia.com/index.php?title=Rs28937893 reference = Chr4 snp rs28937894 6354519..6354519 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6]" http://www.snpedia.com/index.php?title=Rs28937894 reference = Chr4 snp rs28937895 6354915..6354915 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6]" http://www.snpedia.com/index.php?title=Rs28937895 reference = Chr1 snp rs28937896 245654432..245654432 "[omim:FAMILIAL COLD AUTOINFLAMMATORY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28937896 reference = Chr8 snp rs28937897 20156888..20156888 "[omim:ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28937897 reference = Chr19 snp rs28937898 50748773..50748773 "[omim:OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937898 reference = Chr19 snp rs28937899 50748737..50748737 "[omim:OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28937899 reference = Chr19 snp rs28937900 51951373..51951373 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, 2I]" http://www.snpedia.com/index.php?title=Rs28937900 reference = Chr19 snp rs28937901 51951493..51951493 "[omim:MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES]" http://www.snpedia.com/index.php?title=Rs28937901 reference = Chr19 illumina rs28937902 51951210..51951210 "[omim:MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES]" http://www.snpedia.com/index.php?title=Rs28937902 reference = Chr19 illumina rs28937903 51951911..51951911 "[omim:MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES]" http://www.snpedia.com/index.php?title=Rs28937903 reference = Chr19 illumina rs28937904 51951760..51951760 "[omim:MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES]" http://www.snpedia.com/index.php?title=Rs28937904 reference = Chr19 snp rs28937905 51950707..51950707 "[omim:MUSCULAR DYSTROPHY, LIMB-GIRDLE, 2I]" http://www.snpedia.com/index.php?title=Rs28937905 reference = Chr8 snp rs28937906 75438924..75438924 "[omim:CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A]" http://www.snpedia.com/index.php?title=Rs28937906 reference = Chr6 snp rs28937907 51997576..51997576 "[omim:POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28937907 reference = Chr16 snp rs28937908 82490369..82490369 "[omim:MALONYL-CoA DECARBOXYLASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28937908 reference = Chr17 snp rs28937909 75701308..75701308 "[omim:GLYCOGEN STORAGE DISEASE II, ADULT FORM]" http://www.snpedia.com/index.php?title=Rs28937909 reference = Chr11 snp rs28938168 117198349..117198349 "[omim:HYPOMAGNESEMIA 2, RENAL]" http://www.snpedia.com/index.php?title=Rs28938168 reference = Chr10 snp rs28938169 13380242..13380242 "[omim:REFSUM DISEASE]" http://www.snpedia.com/index.php?title=Rs28938169 reference = Chr4 snp rs28938170 2870320..2870320 "[omim:CHERUBISM]" http://www.snpedia.com/index.php?title=Rs28938170 reference = Chr4 snp rs28938171 2870321..2870321 "[omim:CHERUBISM]" http://www.snpedia.com/index.php?title=Rs28938171 reference = Chr12 snp rs28938172 48275668..48275668 "[omim:PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET]" http://www.snpedia.com/index.php?title=Rs28938172 reference = Chr7 snp rs28938173 150703484..150703484 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28938173 reference = Chr11 snp rs28938174 70831013..70831013 "[omim:SMITH-LEMLI-OPITZ SYNDROME]" http://www.snpedia.com/index.php?title=Rs28938174 reference = Chr14 snp rs28938175 30416597..30416597 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 9]" http://www.snpedia.com/index.php?title=Rs28938175 reference = Chr15 snp rs28938176 53309913..53309913 "[omim:GRISCELLI SYNDROME, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28938176 reference = Chr15 snp rs28938468 70814561..70814561 "[omim:BARDET-BIEDL SYNDROME 4]" http://www.snpedia.com/index.php?title=Rs28938468 reference = Chr11 snp rs28938469 17373782..17373782 "[omim:HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1]" http://www.snpedia.com/index.php?title=Rs28938469 reference = Chr3 snp rs28938470 185553292..185553292 "[omim:EPILEPSY, JUVENILE ABSENCE]" http://www.snpedia.com/index.php?title=Rs28938470 reference = Chr13 snp rs28938471 64782191..64782191 "[omim:LIPOID CONGENITAL ADRENAL HYPERPLASIA]" http://www.snpedia.com/index.php?title=Rs28938471 reference = Chr20 snp rs28938472 32988440..32988440 "[omim:GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIA DUE TO]" http://www.snpedia.com/index.php?title=Rs28938472 reference = Chr1 snp rs28938473 94185308..94185308 "[omim:FUNDUS FLAVIMACULATUS]" http://www.snpedia.com/index.php?title=Rs28938473 reference = Chr17 snp rs28938474 56912064..56912064 "[omim:SMALL PATELLA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28938474 reference = ChrNone snp rs28938475 10627051..10627051 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia]" http://www.snpedia.com/index.php?title=Rs28938475 reference = Chr20 snp rs28939068 23563967..23563967 "This snp has now been studied extensively. full text available from [http://www.plosgenetics.org/art..." http://www.snpedia.com/index.php?title=Rs28939068 reference = Chr8 snp rs28939069 116496419..116496419 "[omim:TRICHORHINOPHALANGEAL SYNDROME, TYPE I]" http://www.snpedia.com/index.php?title=Rs28939069 reference = Chr8 snp rs28939070 116496418..116496418 "[omim:TRICHORHINOPHALANGEAL SYNDROME, TYPE I]" http://www.snpedia.com/index.php?title=Rs28939070 reference = Chr14 snp rs28939071 74553549..74553549 "[omim:COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7]" http://www.snpedia.com/index.php?title=Rs28939071 reference = Chr14 snp rs28939072 91427431..91427431 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939072 reference = Chr14 snp rs28939073 91413718..91413718 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939073 reference = Chr14 snp rs28939074 91413682..91413682 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939074 reference = Chr10 snp rs28939075 95546829..95546829 "[omim:EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28939075 reference = Chr2 snp rs28939076 190265434..190265434 "[omim:HEMOCHROMATOSIS, TYPE 4]" http://www.snpedia.com/index.php?title=Rs28939076 reference = Chr3 snp rs28939077 43718966..43718966 "[omim:TRIGLYCERIDE STORAGE DISEASE WITH IMPAIRED LONG-CHAIN FATTY ACID]" http://www.snpedia.com/index.php?title=Rs28939077 reference = Chr3 snp rs28939078 43734171..43734171 "[omim:TRIGLYCERIDE STORAGE DISEASE WITH IMPAIRED LONG-CHAIN FATTY ACID]" http://www.snpedia.com/index.php?title=Rs28939078 reference = Chr6 snp rs28939079 41235589..41235589 "[omim:POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28939079 reference = Chr5 snp rs28939080 14766753..14766753 "[omim:CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28939080 reference = Chr7 snp rs28939081 137851633..137851633 "[omim:RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSET SENSORINEURAL HEARING LOS..." http://www.snpedia.com/index.php?title=Rs28939081 reference = Chr3 snp rs28939082 194838471..194838471 "[omim:OPTIC ATROPHY 1]" http://www.snpedia.com/index.php?title=Rs28939082 reference = Chr3 snp rs28939083 10306457..10306457 "[omim:OBESITY, AGE AT ONSET OF]" http://www.snpedia.com/index.php?title=Rs28939083 reference = Chr21 snp rs28939084 42669030..42669030 "[omim:DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 10]" http://www.snpedia.com/index.php?title=Rs28939084 reference = Chr9 snp rs28939085 96082722..96082722 "[omim:17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28939085 reference = Chr7 snp rs28939086 106924616..106924616 "[omim:PENDRED SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939086 reference = Chr11 snp rs28939087 45784367..45784367 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc]" http://www.snpedia.com/index.php?title=Rs28939087 reference = Chr20 snp rs28939088 3841179..3841179 "[omim:HARP SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939088 reference = Chr15 snp rs28939089 75111700..75111700 "[omim:PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE]" http://www.snpedia.com/index.php?title=Rs28939089 reference = Chr3 snp rs28939091 152173042..152173042 "[omim:USHER SYNDROME, TYPE III]" http://www.snpedia.com/index.php?title=Rs28939091 reference = Chr1 snp rs28939092 55030066..55030066 "[omim:DESMOSTEROLOSIS]" http://www.snpedia.com/index.php?title=Rs28939092 reference = Chr1 snp rs28939093 55052828..55052828 "[omim:DESMOSTEROLOSIS]" http://www.snpedia.com/index.php?title=Rs28939093 reference = Chr14 snp rs28939094 50164601..50164601 "[omim:SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28939094 reference = Chr2 snp rs28939095 222987380..222987380 "[omim:WAARDENBURG SYNDROME, TYPE II]" http://www.snpedia.com/index.php?title=Rs28939095 reference = Chr2 snp rs28939096 222987255..222987255 "[omim:WAARDENBURG SYNDROME, TYPE III]" http://www.snpedia.com/index.php?title=Rs28939096 reference = Chr6 snp rs28939097 43036629..43036629 "[omim:GLYCINE N-METHYLTRANSFERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28939097 reference = Chr3 snp rs28939098 159847387..159847387 "[omim:COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1]" http://www.snpedia.com/index.php?title=Rs28939098 reference = Chr6 snp rs28939099 51997346..51997346 "[omim:POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28939099 reference = Chr17 snp rs28939100 75701744..75701744 "[omim:GLYCOGEN STORAGE DISEASE II, ADULT FORM]" http://www.snpedia.com/index.php?title=Rs28939100 reference = Chr2 snp rs28939368 32273684..32273684 "[omim:SPASTIC PARAPLEGIA 4]" http://www.snpedia.com/index.php?title=Rs28939368 reference = Chr9 snp rs28939369 34503163..34503163 "[omim:KARTAGENER SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939369 reference = Chr14 snp rs28939370 91423350..91423350 "[omim:CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE I]" http://www.snpedia.com/index.php?title=Rs28939370 reference = Chr14 snp rs28939371 91473245..91473245 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939371 reference = Chr14 snp rs28939372 91473211..91473211 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939372 reference = Chr14 snp rs28939373 91473164..91473164 "[omim:MACULAR DEGENERATION, AGE-RELATED, 3]" http://www.snpedia.com/index.php?title=Rs28939373 reference = Chr19 snp rs28939374 43892766..43892766 "[omim:GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 1]" http://www.snpedia.com/index.php?title=Rs28939374 reference = Chr19 snp rs28939375 43892779..43892779 "[omim:GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 1]" http://www.snpedia.com/index.php?title=Rs28939375 reference = Chr19 snp rs28939376 43892787..43892787 "[omim:GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 1]" http://www.snpedia.com/index.php?title=Rs28939376 reference = Chr14 snp rs28939377 102459879..102459879 "[omim:MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE]" http://www.snpedia.com/index.php?title=Rs28939377 reference = Chr3 snp rs28939378 157245287..157245287 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik]" http://www.snpedia.com/index.php?title=Rs28939378 reference = Chr9 snp rs28939379 77049864..77049864 "[omim:CHOREOACANTHOCYTOSIS]" http://www.snpedia.com/index.php?title=Rs28939379 reference = Chr5 snp rs28939380 33987490..33987490 "[omim:OCULOCUTANEOUS ALBINISM, TYPE IV]" http://www.snpedia.com/index.php?title=Rs28939380 reference = Chr15 snp rs28939381 75110621..75110621 "[omim:PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE]" http://www.snpedia.com/index.php?title=Rs28939381 reference = Chr13 snp rs28939382 31249535..31249535 "[omim:CRYPTORCHIDISM, IDIOPATHIC]" http://www.snpedia.com/index.php?title=Rs28939382 reference = Chr6 snp rs28939383 52055958..52055958 "[omim:POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28939383 reference = Chr15 snp rs28939384 66291185..66291185 "[omim:CEROID LIPOFUSCINOSIS, NEURONAL, 6]" http://www.snpedia.com/index.php?title=Rs28939384 reference = Chr20 snp rs28939668 10581181..10581181 "[omim:TETRALOGY OF FALLOT]" http://www.snpedia.com/index.php?title=Rs28939668 reference = Chr12 snp rs28939669 50986288..50986288 "[omim:MONILETHRIX]" http://www.snpedia.com/index.php?title=Rs28939669 reference = Chr10 snp rs28939670 124332299..124332299 "[omim:GLIOBLASTOMA MULTIFORME, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28939670 reference = Chr10 snp rs28939671 13365701..13365701 "[omim:REFSUM DISEASE]" http://www.snpedia.com/index.php?title=Rs28939671 reference = Chr10 snp rs28939672 13370518..13370518 "[omim:REFSUM DISEASE]" http://www.snpedia.com/index.php?title=Rs28939672 reference = Chr10 snp rs28939673 13370434..13370434 "[omim:REFSUM DISEASE]" http://www.snpedia.com/index.php?title=Rs28939673 reference = Chr10 snp rs28939674 13365700..13365700 "[omim:REFSUM DISEASE]" http://www.snpedia.com/index.php?title=Rs28939674 reference = Chr22 snp rs28939675 18125350..18125350 "[omim:CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939675 reference = Chr2 snp rs28939676 20124558..20124558 "[omim:HAND OSTEOARTHRITIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs28939676 reference = Chr2 snp rs28939677 20069120..20069120 "[omim:MULTIPLE EPIPHYSEAL DYSPLASIA, MATN3-RELATED]" http://www.snpedia.com/index.php?title=Rs28939677 reference = Chr7 snp rs28939678 91778777..91778777 "[omim:ZELLWEGER SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939678 reference = Chr11 snp rs28939679 67557190..67557190 "[omim:LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28939679 reference = ChrX snp rs28939680 48977522..48977522 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F]" http://www.snpedia.com/index.php?title=Rs28939680 reference = ChrX snp rs28939681 48977520..48977520 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F]" http://www.snpedia.com/index.php?title=Rs28939681 reference = Chr19 snp rs28939682 53031450..53031450 "[omim:CONE-ROD DYSTROPHY 2]" http://www.snpedia.com/index.php?title=Rs28939682 reference = Chr20 snp rs28939683 61541471..61541471 "[omim:EPILEPSY, BENIGN NEONATAL, 1]" http://www.snpedia.com/index.php?title=Rs28939683 reference = Chr20 snp rs28939684 61546506..61546506 "[omim:EPILEPSY, BENIGN NEONATAL, 1]" http://www.snpedia.com/index.php?title=Rs28939684 reference = Chr18 snp rs28939685 53513418..53513418 "[omim:CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1]" http://www.snpedia.com/index.php?title=Rs28939685 reference = Chr18 snp rs28939686 53487663..53487663 "[omim:CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1]" http://www.snpedia.com/index.php?title=Rs28939686 reference = Chr10 snp rs28939688 13191276..13191276 "[omim:GLAUCOMA 1, OPEN ANGLE, E]" http://www.snpedia.com/index.php?title=Rs28939688 reference = Chr10 snp rs28939689 13218772..13218772 "[omim:GLAUCOMA 1, OPEN ANGLE, E]" http://www.snpedia.com/index.php?title=Rs28939689 reference = Chr11 snp rs28939690 120543995..120543995 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 8]" http://www.snpedia.com/index.php?title=Rs28939690 reference = Chr11 snp rs28939691 120536220..120536220 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 12]" http://www.snpedia.com/index.php?title=Rs28939691 reference = Chr9 snp rs28939692 128495350..128495350 "[omim:NAIL-PATELLA SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939692 reference = Chr19 snp rs28939693 51332337..51332337 "[omim:HOLOPROSENCEPHALY 4]" http://www.snpedia.com/index.php?title=Rs28939693 reference = Chr7 snp rs28939694 2038402..2038402 "[omim:PROSTATE CANCER, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28939694 reference = Chr19 snp rs28939695 41030884..41030884 "[omim:NEPHROSIS 1, CONGENITAL, FINNISH TYPE]" http://www.snpedia.com/index.php?title=Rs28939695 reference = Chr16 snp rs28939696 59247051..59247051 "[omim:RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28939696 reference = Chr16 snp rs28939697 59247052..59247052 "[omim:RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2]" http://www.snpedia.com/index.php?title=Rs28939697 reference = Chr11 snp rs28939698 70827660..70827660 "[omim:SMITH-LEMLI-OPITZ SYNDROME]" http://www.snpedia.com/index.php?title=Rs28939698 reference = Chr10 snp rs28939699 17123165..17123165 "[omim:MEGALOBLASTIC ANEMIA 1, FINNISH TYPE]" http://www.snpedia.com/index.php?title=Rs28939699 reference = Chr2 snp rs28939700 71709489..71709489 "[omim:MIYOSHI MYOPATHY]" http://www.snpedia.com/index.php?title=Rs28939700 reference = Chr16 snp rs28939701 16164445..16164445 "[omim:PSEUDOXANTHOMA ELASTICUM]" http://www.snpedia.com/index.php?title=Rs28939701 reference = Chr16 snp rs28939702 16156257..16156257 "[omim:PSEUDOXANTHOMA ELASTICUM]" http://www.snpedia.com/index.php?title=Rs28939702 reference = Chr4 snp rs28939703 96408204..96408204 "[omim:BRACHYDACTYLY, TYPE A2]" http://www.snpedia.com/index.php?title=Rs28939703 reference = Chr4 snp rs28939704 96432949..96432949 "[omim:BRACHYDACTYLY, TYPE A2]" http://www.snpedia.com/index.php?title=Rs28939704 reference = Chr5 snp rs28939705 131747872..131747872 "[omim:CARNITINE DEFICIENCY, SYSTEMIC PRIMARY]" http://www.snpedia.com/index.php?title=Rs28939705 reference = Chr3 snp rs28939706 58096830..58096830 "[omim:LARSEN SYNDROME, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28939706 reference = Chr12 snp rs28939707 50581211..50581211 "[omim:ATELOSTEOGENESIS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28939707 reference = Chr11 snp rs28939708 67934120..67934120 "[omim:EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28939708 reference = Chr11 snp rs28939709 67961031..67961031 "[omim:EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28939709 reference = Chr1 snp rs28939710 40954945..40954945 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2]" http://www.snpedia.com/index.php?title=Rs28939710 reference = Chr10 snp rs28939711 101473804..101473804 "[omim:CARDIOMYOPATHY, HYPERTROPHIC, EARLY-ONSET FATAL]" http://www.snpedia.com/index.php?title=Rs28939711 reference = Chr9 snp rs28939712 108735897..108735897 "[omim:FAMILIAL DYSAUTONOMIA]" http://www.snpedia.com/index.php?title=Rs28939712 reference = Chr9 snp rs28939713 36208224..36208224 "[omim:NONAKA MYOPATHY]" http://www.snpedia.com/index.php?title=Rs28939713 reference = Chr11 snp rs28939714 47560268..47560268 "[omim:LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28939714 reference = Chr4 snp rs28939715 41444256..41444256 "[omim:NEUROBLASTOMA]" http://www.snpedia.com/index.php?title=Rs28939715 reference = Chr4 snp rs28939716 41590302..41590302 "[omim:HIRSCHSPRUNG DISEASE WITH NEUROBLASTOMA]" http://www.snpedia.com/index.php?title=Rs28939716 reference = Chr3 snp rs28939717 185337177..185337177 "[omim:LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER]" http://www.snpedia.com/index.php?title=Rs28939717 reference = Chr19 snp rs28939719 870563..870563 "[omim:HYPOGONADOTROPIC HYPOGONADISM]" http://www.snpedia.com/index.php?title=Rs28939719 reference = Chr1 snp rs28939720 195663312..195663312 "[omim:RETINITIS PIGMENTOSA 12]" http://www.snpedia.com/index.php?title=Rs28939720 reference = Chr2 snp rs28940268 215676793..215676793 "[omim:ICHTHYOSIS, LAMELLAR 2]" http://www.snpedia.com/index.php?title=Rs28940268 reference = Chr2 snp rs28940269 215676796..215676796 "[omim:ICHTHYOSIS, LAMELLAR 2]" http://www.snpedia.com/index.php?title=Rs28940269 reference = Chr2 snp rs28940270 215672455..215672455 "[omim:ICHTHYOSIS, LAMELLAR 2]" http://www.snpedia.com/index.php?title=Rs28940270 reference = Chr2 snp rs28940271 215670838..215670838 "[omim:ICHTHYOSIS, LAMELLAR 2]" http://www.snpedia.com/index.php?title=Rs28940271 reference = Chr8 snp rs28940272 100901435..100901435 "[omim:COHEN SYNDROME]" http://www.snpedia.com/index.php?title=Rs28940272 reference = Chr11 snp rs28940273 61479797..61479797 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28940273 reference = Chr11 snp rs28940274 61479771..61479771 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28940274 reference = Chr11 snp rs28940275 61475870..61475870 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28940275 reference = Chr11 snp rs28940276 61475879..61475879 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28940276 reference = Chr11 snp rs28940278 61475994..61475994 "[omim:VITELLIFORM MACULAR DYSTROPHY, ADULT-ONSET]" http://www.snpedia.com/index.php?title=Rs28940278 reference = Chr17 snp rs28940279 3349044..3349044 "[omim:CANAVAN DISEASE]" http://www.snpedia.com/index.php?title=Rs28940279 reference = Chr13 snp rs28940280 76472716..76472716 "[omim:CEROID LIPOFUSCINOSIS, NEURONAL, 5]" http://www.snpedia.com/index.php?title=Rs28940280 reference = Chr8 snp rs28940281 1818242..1818242 "[omim:SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28940281 reference = Chr17 snp rs28940282 67630516..67630516 "[omim:ACAMPOMELIC CAMPOMELIC DYSPLASIA]" http://www.snpedia.com/index.php?title=Rs28940282 reference = Chr2 snp rs28940283 211164862..211164862 "[omim:CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940283 reference = Chr1 snp rs28940284 20716325..20716325 "[omim:PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET]" http://www.snpedia.com/index.php?title=Rs28940284 reference = Chr1 snp rs28940285 20717439..20717439 "[omim:PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET]" http://www.snpedia.com/index.php?title=Rs28940285 reference = Chr7 snp rs28940286 65001703..65001703 "[omim:ARGININOSUCCINIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28940286 reference = Chr7 snp rs28940287 65001215..65001215 "[omim:ARGININOSUCCINIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28940287 reference = Chr19 snp rs28940288 46619992..46619992 "[omim:MAPLE SYRUP URINE DISEASE, INTERMEDIATE, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940288 reference = Chr19 snp rs28940289 48707447..48707447 "[omim:ETHYLMALONIC ENCEPHALOPATHY]" http://www.snpedia.com/index.php?title=Rs28940289 reference = Chr9 snp rs28940290 132186424..132186424 "[omim:ATAXIA-OCULAR APRAXIA 2]" http://www.snpedia.com/index.php?title=Rs28940290 reference = Chr1 snp rs28940291 11986983..11986983 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940291 reference = Chr1 snp rs28940292 12005833..12005833 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940292 reference = Chr1 snp rs28940293 11986929..11986929 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940293 reference = Chr1 snp rs28940294 11995746..11995746 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940294 reference = Chr1 snp rs28940295 11993353..11993353 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940295 reference = Chr1 snp rs28940296 11986907..11986907 "[omim:CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2]" http://www.snpedia.com/index.php?title=Rs28940296 reference = Chr1 snp rs28940297 154535172..154535172 "[omim:RENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS]" http://www.snpedia.com/index.php?title=Rs28940297 reference = Chr3 snp rs28940298 10166605..10166605 "[omim:POLYCYTHEMIA, CHUVASH TYPE]" http://www.snpedia.com/index.php?title=Rs28940298 reference = Chr3 snp rs28940300 10166581..10166581 "[omim:ERYTHROCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28940300 reference = Chr3 snp rs28940301 10166578..10166578 "[omim:ERYTHROCYTOSIS, FAMILIAL, 2]" http://www.snpedia.com/index.php?title=Rs28940301 reference = Chr16 illumina rs28940302 31013467..31013467 "[omim:WARFARIN RESISTANCE]" http://www.snpedia.com/index.php?title=Rs28940302 reference = Chr16 snp rs28940303 31013418..31013418 "[omim:WARFARIN RESISTANCE]" http://www.snpedia.com/index.php?title=Rs28940303 reference = Chr16 snp rs28940304 31013380..31013380 "[omim:WARFARIN RESISTANCE]" http://www.snpedia.com/index.php?title=Rs28940304 reference = Chr16 snp rs28940305 31010065..31010065 "[omim:WARFARIN RESISTANCE]" http://www.snpedia.com/index.php?title=Rs28940305 reference = Chr19 snp rs28940306 55466493..55466493 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4]" http://www.snpedia.com/index.php?title=Rs28940306 reference = Chr19 snp rs28940307 55454279..55454279 "[omim:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4]" http://www.snpedia.com/index.php?title=Rs28940307 reference = Chr22 snp rs28940308 16937228..16937228 "[omim:ZELLWEGER SYNDROME]" http://www.snpedia.com/index.php?title=Rs28940308 reference = Chr12 snp rs28940309 114942034..114942034 "[omim:TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED]" http://www.snpedia.com/index.php?title=Rs28940309 reference = Chr12 snp rs28940310 114897475..114897475 "[omim:TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED]" http://www.snpedia.com/index.php?title=Rs28940310 reference = Chr6 snp rs28940311 52425556..52425556 "[omim:MYOCLONIC EPILEPSY, JUVENILE, 1]" http://www.snpedia.com/index.php?title=Rs28940311 reference = Chr6 snp rs28940312 52426885..52426885 "[omim:MYOCLONIC EPILEPSY, JUVENILE, 1]" http://www.snpedia.com/index.php?title=Rs28940312 reference = Chr14 snp rs28940313 67265679..67265679 "[omim:LEBER CONGENITAL AMAUROSIS, TYPE III]" http://www.snpedia.com/index.php?title=Rs28940313 reference = Chr14 snp rs28940314 67261020..67261020 "[omim:LEBER CONGENITAL AMAUROSIS, TYPE III]" http://www.snpedia.com/index.php?title=Rs28940314 reference = Chr14 snp rs28940315 67261676..67261676 "[omim:LEBER CONGENITAL AMAUROSIS, TYPE III]" http://www.snpedia.com/index.php?title=Rs28940315 reference = Chr2 snp rs28940568 215551799..215551799 "[omim:ICHTHYOSIS, LAMELLAR 2]" http://www.snpedia.com/index.php?title=Rs28940568 reference = Chr8 snp rs28940569 1716068..1716068 "[omim:CEROID LIPOFUSCINOSIS, NEURONAL, 8]" http://www.snpedia.com/index.php?title=Rs28940569 reference = Chr11 snp rs28940570 61482207..61482207 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28940570 reference = Chr22 snp rs28940571 41419150..41419150 "[omim:P BLOOD GROUP SYSTEM, p PHENOTYPE]" http://www.snpedia.com/index.php?title=Rs28940571 reference = Chr22 snp rs28940572 41419342..41419342 "[omim:P BLOOD GROUP SYSTEM, p PHENOTYPE]" http://www.snpedia.com/index.php?title=Rs28940572 reference = Chr11 snp rs28940573 6594853..6594853 "[omim:CEROID LIPOFUSCINOSIS, NEURONAL, 2]" http://www.snpedia.com/index.php?title=Rs28940573 reference = Chr17 snp rs28940574 3349104..3349104 "[omim:CANAVAN DISEASE]" http://www.snpedia.com/index.php?title=Rs28940574 reference = Chr6 snp rs28940575 18230741..18230741 "[omim:EPILEPSY, PROGRESSIVE MYOCLONIC 2B]" http://www.snpedia.com/index.php?title=Rs28940575 reference = Chr6 snp rs28940576 18230612..18230612 "[omim:EPILEPSY, PROGRESSIVE MYOCLONIC 2B]" http://www.snpedia.com/index.php?title=Rs28940576 reference = Chr16 snp rs28940577 3233411..3233411 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs28940577 reference = Chr16 snp rs28940578 3233406..3233406 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs28940578 reference = Chr16 snp rs28940579 3233311..3233311 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs28940579 reference = Chr16 snp rs28940580 3233448..3233448 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs28940580 reference = Chr16 snp rs28940581 3233533..3233533 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs28940581 reference = Chr6 snp rs28940582 31937838..31937838 "[omim:SIALIDOSIS, TYPE II]" http://www.snpedia.com/index.php?title=Rs28940582 reference = Chr6 snp rs28940583 31936344..31936344 "[omim:SIALIDOSIS, TYPE I]" http://www.snpedia.com/index.php?title=Rs28940583 reference = Chr6 illumina rs28940584 31936319..31936319 "[omim:SIALIDOSIS, TYPE II]" http://www.snpedia.com/index.php?title=Rs28940584 reference = Chr7 snp rs28940585 65184865..65184865 "[omim:ARGININOSUCCINIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28940585 reference = Chr1 snp rs28940586 144126776..144126776 "[omim:HEMOCHROMATOSIS, TYPE 2A]" http://www.snpedia.com/index.php?title=Rs28940586 reference = Chr11 snp rs28940587 64275515..64275515 "[omim:MCARDLE DISEASE]" http://www.snpedia.com/index.php?title=Rs28940587 reference = Chr3 snp rs28940588 185446041..185446041 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id]" http://www.snpedia.com/index.php?title=Rs28940588 reference = Chr11 snp rs28940589 66375991..66375991 "[omim:PYRUVATE CARBOXYLASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940589 reference = Chr11 snp rs28940590 66374965..66374965 "[omim:PYRUVATE CARBOXYLASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940590 reference = Chr11 illumina rs28940591 66395415..66395415 "[omim:PYRUVATE CARBOXYLASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940591 reference = Chr17 snp rs28940868 75701316..75701316 "[omim:GLYCOGEN STORAGE DISEASE II, INFANTILE FORM]" http://www.snpedia.com/index.php?title=Rs28940868 reference = Chr1 snp rs28940869 46430656..46430656 "[omim:MUSCLE-EYE-BRAIN DISEASE]" http://www.snpedia.com/index.php?title=Rs28940869 reference = Chr11 snp rs28940870 57138523..57138523 "[omim:ANGIOEDEMA, HEREDITARY, TYPE II]" http://www.snpedia.com/index.php?title=Rs28940870 reference = Chr15 snp rs28940871 70425700..70425700 "[omim:TAY-SACHS DISEASE]" http://www.snpedia.com/index.php?title=Rs28940871 reference = Chr12 snp rs28940872 119661542..119661542 "[omim:SCAD DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940872 reference = Chr12 snp rs28940874 119660125..119660125 "[omim:SCAD DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940874 reference = Chr11 snp rs28940876 88551011..88551011 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940876 reference = Chr11 snp rs28940877 88551034..88551034 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940877 reference = Chr11 snp rs28940878 88550894..88550894 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940878 reference = Chr11 snp rs28940879 88550933..88550933 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940879 reference = Chr11 snp rs28940880 88551385..88551385 "[omim:ALBINISM, OCULOCUTANEOUS, TYPE IA]" http://www.snpedia.com/index.php?title=Rs28940880 reference = Chr11 snp rs28940881 88550770..88550770 "[omim:ALBINISM, OCULAR, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs28940881 reference = Chr1 snp rs28940882 23997276..23997276 "[omim:GALACTOSE EPIMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940882 reference = Chr1 snp rs28940883 23997237..23997237 "[omim:GALACTOSE EPIMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940883 reference = Chr1 illumina rs28940884 23995799..23995799 "[omim:GALACTOSE EPIMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940884 reference = Chr1 snp rs28940885 23995260..23995260 "[omim:GALACTOSE EPIMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940885 reference = Chr16 snp rs28940886 66534343..66534343 "[omim:LCAT DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940886 reference = Chr16 snp rs28940887 66534123..66534123 "[omim:LCAT DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940887 reference = Chr16 snp rs28940888 66531597..66531597 "[omim:LCAT DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28940888 reference = Chr15 snp rs28940889 38494945..38494945 "[omim:ISOVALERIC ACIDEMIA]" http://www.snpedia.com/index.php?title=Rs28940889 reference = Chr11 snp rs28940890 31779710..31779710 "[omim:ECTOPIA PUPILLAE]" http://www.snpedia.com/index.php?title=Rs28940890 reference = Chr1 snp rs28940891 5857593..5857593 "[omim:NEPHRONOPHTHISIS 4, JUVENILE]" http://www.snpedia.com/index.php?title=Rs28940891 reference = Chr18 snp rs28940892 13874757..13874757 "[omim:GLUCOCORTICOID DEFICIENCY 1]" http://www.snpedia.com/index.php?title=Rs28940892 reference = Chr22 illumina rs28940893 49410686..49410686 "[omim:ARYLSULFATASE A, ALLELE A]" http://www.snpedia.com/index.php?title=Rs28940893 reference = Chr22 snp rs28940894 49411565..49411565 "[omim:METACHROMATIC LEUKODYSTROPHY, ADULT]" http://www.snpedia.com/index.php?title=Rs28940894 reference = Chr22 illumina rs28940895 49410740..49410740 "[omim:METACHROMATIC LEUKODYSTROPHY, ADULT]" http://www.snpedia.com/index.php?title=Rs28940895 reference = Chr17 snp rs28940896 36981293..36981293 "[omim:PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, WITH KNUCKLE PADS]" http://www.snpedia.com/index.php?title=Rs28940896 reference = Chr18 snp rs28940897 19373785..19373785 "[omim:NIEMANN-PICK DISEASE, TYPE C1]" http://www.snpedia.com/index.php?title=Rs28940897 reference = Chr11 snp rs28941468 61483574..61483574 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28941468 reference = Chr11 snp rs28941469 61481477..61481477 "[omim:BEST MACULAR DYSTROPHY]" http://www.snpedia.com/index.php?title=Rs28941469 reference = Chr10 snp rs28941470 27490065..27490065 "[omim:THROMBOCYTOPENIA 2]" http://www.snpedia.com/index.php?title=Rs28941470 reference = Chr22 snp rs28941471 39079454..39079454 "[omim:ADENYLOSUCCINASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28941471 reference = Chr7 snp rs28941472 65191536..65191536 "[omim:ARGININOSUCCINIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28941472 reference = Chr7 snp rs28941473 64995888..64995888 "[omim:ARGININOSUCCINIC ACIDURIA]" http://www.snpedia.com/index.php?title=Rs28941473 reference = Chr6 snp rs28941474 131936147..131936147 "[omim:ARGININEMIA]" http://www.snpedia.com/index.php?title=Rs28941474 reference = Chr9 snp rs28941475 132254362..132254362 "[omim:AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE]" http://www.snpedia.com/index.php?title=Rs28941475 reference = Chr16 snp rs28941476 87242012..87242012 "[omim:GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE]" http://www.snpedia.com/index.php?title=Rs28941476 reference = Chr7 snp rs28941477 72082614..72082614 "[omim:GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I]" http://www.snpedia.com/index.php?title=Rs28941477 reference = Chr21 snp rs28941768 46396287..46396287 "[omim:GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28941768 reference = Chr5 snp rs28941769 149720952..149720952 "[omim:TREACHER COLLINS SYNDROME]" http://www.snpedia.com/index.php?title=Rs28941769 reference = Chr15 snp rs28941770 70432500..70432500 "[omim:TAY-SACHS DISEASE]" http://www.snpedia.com/index.php?title=Rs28941770 reference = Chr15 snp rs28941771 70432495..70432495 "[omim:GM2-GANGLIOSIDOSIS, LATE ONSET]" http://www.snpedia.com/index.php?title=Rs28941771 reference = Chr5 snp rs28941772 74052709..74052709 "[omim:HEXOSAMINIDASE B, HEAT-LABILE POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs28941772 reference = Chr12 snp rs28941773 119661354..119661354 "[omim:SCAD DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28941773 reference = Chr10 snp rs28941774 127493640..127493640 "[omim:PORPHYRIA, CONGENITAL ERYTHROPOIETIC]" http://www.snpedia.com/index.php?title=Rs28941774 reference = Chr10 snp rs28941775 127493653..127493653 "[omim:PORPHYRIA, CONGENITAL ERYTHROPOIETIC]" http://www.snpedia.com/index.php?title=Rs28941775 reference = Chr19 snp rs28941776 11087829..11087829 "[omim:FH GENOA]" http://www.snpedia.com/index.php?title=Rs28941776 reference = Chr11 snp rs28941777 32370175..32370175 "[omim:MESANGIAL SCLEROSIS, ISOLATED DIFFUSE]" http://www.snpedia.com/index.php?title=Rs28941777 reference = Chr11 snp rs28941778 32370136..32370136 "[omim:MESANGIAL SCLEROSIS, ISOLATED DIFFUSE]" http://www.snpedia.com/index.php?title=Rs28941778 reference = Chr11 snp rs28941779 32370148..32370148 "[omim:FRASIER SYNDROME]" http://www.snpedia.com/index.php?title=Rs28941779 reference = Chr3 snp rs28941780 9954308..9954308 "[omim:ATRIOVENTRICULAR SEPTAL DEFECT, PARTIAL, WITH HETEROTAXY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28941780 reference = Chr3 snp rs28941781 46725682..46725682 "[omim:DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 6]" http://www.snpedia.com/index.php?title=Rs28941781 reference = Chr9 snp rs28941782 133371425..133371425 "[omim:WALKER-WARBURG SYNDROME]" http://www.snpedia.com/index.php?title=Rs28941782 reference = Chr3 snp rs28941783 121848578..121848578 "[omim:ALKAPTONURIA]" http://www.snpedia.com/index.php?title=Rs28941783 reference = Chr12 snp rs28941784 108461593..108461593 "[omim:METHYLMALONIC ACIDURIA, cblB TYPE]" http://www.snpedia.com/index.php?title=Rs28941784 reference = Chr1 snp rs28941785 70593691..70593691 "[omim:CYSTATHIONINURIA]" http://www.snpedia.com/index.php?title=Rs28941785 reference = Chr1 snp rs28941786 70608092..70608092 "[omim:CYSTATHIONINURIA]" http://www.snpedia.com/index.php?title=Rs28941786 reference = Chr1 snp rs28942068 46369851..46369851 "[omim:MUSCLE-EYE-BRAIN DISEASE]" http://www.snpedia.com/index.php?title=Rs28942068 reference = Chr9 snp rs28942069 70840521..70840521 "[omim:FRIEDREICH ATAXIA]" http://www.snpedia.com/index.php?title=Rs28942069 reference = Chr9 illumina rs28942070 126770510..126770510 "[omim:FRIEDREICH ATAXIA]" http://www.snpedia.com/index.php?title=Rs28942070 reference = Chr15 snp rs28942071 70424857..70424857 "[omim:GM2-GANGLIOSIDOSIS, CHRONIC]" http://www.snpedia.com/index.php?title=Rs28942071 reference = Chr15 snp rs28942072 70428488..70428488 "[omim:GM2-GANGLIOSIDOSIS, SUBACUTE]" http://www.snpedia.com/index.php?title=Rs28942072 reference = Chr5 snp rs28942073 74050385..74050385 "[omim:SANDHOFF DISEASE, JUVENILE TYPE]" http://www.snpedia.com/index.php?title=Rs28942073 reference = Chr13 snp rs28942074 51430470..51430470 "[omim:WILSON DISEASE]" http://www.snpedia.com/index.php?title=Rs28942074 reference = Chr13 snp rs28942075 51430510..51430510 "[omim:WILSON DISEASE]" http://www.snpedia.com/index.php?title=Rs28942075 reference = Chr13 snp rs28942076 51421837..51421837 "[omim:WILSON DISEASE]" http://www.snpedia.com/index.php?title=Rs28942076 reference = Chr1 snp rs28942077 232255545..232255545 "[omim:CHEDIAK-HIGASHI SYNDROME, ADULT TYPE]" http://www.snpedia.com/index.php?title=Rs28942077 reference = Chr19 snp rs28942078 11085052..11085052 "[omim:FH AFRIKANER 2]" http://www.snpedia.com/index.php?title=Rs28942078 reference = Chr19 snp rs28942079 11085058..11085058 "[omim:FH ALGERIA]" http://www.snpedia.com/index.php?title=Rs28942079 reference = Chr19 snp rs28942080 11085419..11085419 "[omim:FH KUWAIT]" http://www.snpedia.com/index.php?title=Rs28942080 reference = Chr19 snp rs28942081 11087820..11087820 "[omim:FH SAINT OMER]" http://www.snpedia.com/index.php?title=Rs28942081 reference = Chr19 snp rs28942082 11087877..11087877 "[omim:FH NAPLES]" http://www.snpedia.com/index.php?title=Rs28942082 reference = Chr19 snp rs28942083 11092058..11092058 "[omim:FH FRENCH CANADIAN 2]" http://www.snpedia.com/index.php?title=Rs28942083 reference = Chr19 snp rs28942084 11092112..11092112 "[omim:FH ZAMBIA]" http://www.snpedia.com/index.php?title=Rs28942084 reference = Chr19 snp rs28942085 11101282..11101282 "[omim:FH BARI]" http://www.snpedia.com/index.php?title=Rs28942085 reference = Chr19 snp rs28942086 11087873..11087873 "[omim:FH AARHUS]" http://www.snpedia.com/index.php?title=Rs28942086 reference = Chr16 snp rs28942087 66533817..66533817 "[omim:LCAT DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs28942087 reference = Chr10 snp rs28942088 104253943..104253943 "[omim:MEDULLOBLASTOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs28942088 reference = Chr11 snp rs28942089 32370794..32370794 "[omim:MESANGIAL SCLEROSIS, ISOLATED DIFFUSE]" http://www.snpedia.com/index.php?title=Rs28942089 reference = Chr22 snp rs28942090 48690131..48690131 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig]" http://www.snpedia.com/index.php?title=Rs28942090 reference = Chr3 snp rs28942091 9960136..9960136 "[omim:ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2]" http://www.snpedia.com/index.php?title=Rs28942091 reference = Chr3 snp rs28942092 9960083..9960083 "[omim:ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2]" http://www.snpedia.com/index.php?title=Rs28942092 reference = Chr1 snp rs28942093 206363149..206363149 "[omim:VAN DER WOUDE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28942093 reference = Chr1 snp rs28942094 206363138..206363138 "[omim:VAN DER WOUDE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28942094 reference = Chr1 snp rs28942095 206350366..206350366 "[omim:VAN DER WOUDE SYNDROME]" http://www.snpedia.com/index.php?title=Rs28942095 reference = Chr3 snp rs28942096 46725649..46725649 "[omim:DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 6]" http://www.snpedia.com/index.php?title=Rs28942096 reference = Chr3 snp rs28942097 46725658..46725658 "[omim:DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 6]" http://www.snpedia.com/index.php?title=Rs28942097 reference = Chr1 illumina rs28942098 191357956..191357956 "[omim:HYPERPARATHYROIDISM-JAW TUMOR SYNDROME]" http://www.snpedia.com/index.php?title=Rs28942098 reference = Chr7 snp rs28942099 66097816..66097816 "[omim:SHWACHMAN-DIAMOND SYNDROME]" http://www.snpedia.com/index.php?title=Rs28942099 reference = Chr3 snp rs28942100 121845942..121845942 "[omim:ALKAPTONURIA]" http://www.snpedia.com/index.php?title=Rs28942100 reference = Chr18 snp rs28942104 19370773..19370773 "[omim:NIEMANN-PICK DISEASE, TYPE C1]" http://www.snpedia.com/index.php?title=Rs28942104 reference = Chr18 snp rs28942105 19369441..19369441 "[omim:NIEMANN-PICK DISEASE, TYPE C1]" http://www.snpedia.com/index.php?title=Rs28942105 reference = Chr18 snp rs28942106 19369645..19369645 "[omim:NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM]" http://www.snpedia.com/index.php?title=Rs28942106 reference = Chr18 snp rs28942107 19370776..19370776 "[omim:NIEMANN-PICK DISEASE, TYPE C1]" http://www.snpedia.com/index.php?title=Rs28942107 reference = Chr18 snp rs28942108 19372613..19372613 "[omim:NIEMANN-PICK DISEASE, TYPE C1]" http://www.snpedia.com/index.php?title=Rs28942108 reference = Chr5 snp rs28942109 133972032..133972032 "[omim:CHYLOMICRON RETENTION DISEASE]" http://www.snpedia.com/index.php?title=Rs28942109 reference = Chr5 snp rs28942110 133970599..133970599 "[omim:CHYLOMICRON RETENTION DISEASE]" http://www.snpedia.com/index.php?title=Rs28942110 reference = Chr1 snp rs28942111 55221710..55221710 "[omim:HYPERCHOLESTEROLEMIA, FAMILIAL, 3]" http://www.snpedia.com/index.php?title=Rs28942111 reference = Chr1 snp rs28942112 55230094..55230094 "[omim:HYPERCHOLESTEROLEMIA, FAMILIAL, 3]" http://www.snpedia.com/index.php?title=Rs28942112 reference = Chr6 snp rs28942113 27483700..27483700 "[omim:FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF]" http://www.snpedia.com/index.php?title=Rs28942113 reference = Chr6 snp rs28942114 27483720..27483720 "[omim:FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF]" http://www.snpedia.com/index.php?title=Rs28942114 reference = Chr15 illumina rs28989181 38292136..38292136 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989181 reference = Chr15 snp rs28989182 38292047..38292047 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989182 reference = Chr15 illumina rs28989183 38297073..38297073 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989183 reference = Chr15 illumina rs28989185 38300134..38300134 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989185 reference = Chr15 snp rs28989186 38256165..38256165 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989186 reference = Chr15 illumina rs28989187 38282102..38282102 "[omim:MOSAIC VARIEGATED ANEUPLOIDY SYNDROME]" http://www.snpedia.com/index.php?title=Rs28989187 reference = Chr2 illumina rs28997576 215325423..215325423 "[omim:BREAST CANCER, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs28997576 reference = Chr17 snp rs28999110 4745145..4745145 "[omim:MYASTHENIC SYNDROME, SLOW-CHANNEL CONGENITAL]" http://www.snpedia.com/index.php?title=Rs28999110 reference = ChrNone snp rs28999111 77093621..77093621 "[omim:DEAFNESS, AUTOSOMAL DOMINANT 20]" http://www.snpedia.com/index.php?title=Rs28999111 reference = ChrNone snp rs28999112 77092699..77092699 "[omim:DEAFNESS, AUTOSOMAL DOMINANT 20]" http://www.snpedia.com/index.php?title=Rs28999112 reference = Chr16 snp rs28999113 87403743..87403743 "[omim:APRT DEFICIENCY, JAPANESE TYPE]" http://www.snpedia.com/index.php?title=Rs28999113 reference = Chr4 snp rs28999114 186303111..186303111 "[omim:PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 2]" http://www.snpedia.com/index.php?title=Rs28999114 reference = Chr9 snp rs28999968 124345050..124345050 "[omim:SEX REVERSAL, XY, WITH ADRENAL FAILURE]" http://www.snpedia.com/index.php?title=Rs28999968 reference = Chr3 snp rs28999969 24144144..24144144 "[omim:THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28999969 reference = Chr3 snp rs28999970 24144104..24144104 "[omim:THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT]" http://www.snpedia.com/index.php?title=Rs28999970 reference = Chr3 snp rs29001566 130735244..130735244 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs29001566 reference = ChrX illumina rs29001571 48977547..48977547 "[omim:NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB]" http://www.snpedia.com/index.php?title=Rs29001571 reference = Chr9 snp rs29001584 134195640..134195640 "[omim:AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE]" http://www.snpedia.com/index.php?title=Rs29001584 reference = Chr18 illumina rs29001611 43411123..43411123 "[omim:THIOPURINE S-METHYLTRANSFERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs29001611 reference = Chr3 snp rs29001637 130735243..130735243 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs29001637 reference = Chr3 snp rs29001653 130734255..130734255 "[omim:RETINITIS PIGMENTOSA 4]" http://www.snpedia.com/index.php?title=Rs29001653 reference = Chr9 snp rs29001665 134196501..134196501 "[omim:ATAXIA-OCULAR APRAXIA 2]" http://www.snpedia.com/index.php?title=Rs29001665 reference = Chr9 illumina rs2900180 122746203..122746203 "rs2900180 increases susceptibility to Rheumatoid Arthritis 1.34 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs2900180 reference = Chr15 affy rs2903265 78200439..78200439 "rs2903265 has been reported in a large study to be associated with type-2 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs2903265 reference = Chr22 snp rs2904551 17285934..17285934 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs2904551 reference = Chr22 snp rs2904552 17285964..17285964 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs2904552 reference = Chr5 affy rs2910164 159844996..159844996 "(C;C) predisposes to papillary thyroid carcinoma. Among 42 patients with familial breast cancer and ..." http://www.snpedia.com/index.php?title=Rs2910164 reference = Chr5 illumina rs2918419 142702546..142702546 "Associated with insulin resistance in men Associated with bone mineral density and thus osteoporosi..." http://www.snpedia.com/index.php?title=Rs2918419 reference = Chr15 affy rs2930291 72391887..72391887 "rs2930291 has been reported in a large study to be associated with type-2 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs2930291 reference = Chr2 affy rs2943634 226776324..226776324 "rs2943634 is a SNP found to be reproducibly associated with heart disease" http://www.snpedia.com/index.php?title=Rs2943634 reference = Chr2 affy rs2953145 241164269..241164269 "rs2953145 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs2953145 reference = Chr18 affy rs2957137 58217868..58217868 "rs2957137 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteopor..." http://www.snpedia.com/index.php?title=Rs2957137 reference = Chr11 illumina rs2959656 64328594..64328594 "" http://www.snpedia.com/index.php?title=Rs2959656 reference = Chr5 snp rs2963238 1497427..1497427 "rs2963238, a SNP in the dopamine transporter SLC6A3 gene, has been associated along with several oth..." http://www.snpedia.com/index.php?title=Rs2963238 reference = Chr7 both rs2974938 113305738..113305738 "" http://www.snpedia.com/index.php?title=Rs2974938 reference = Chr7 illumina rs2974942 113307032..113307032 "" http://www.snpedia.com/index.php?title=Rs2974942 reference = Chr7 snp rs2974944 113306955..113306955 "" http://www.snpedia.com/index.php?title=Rs2974944 reference = Chr2 illumina rs2975766 241186747..241186747 "" http://www.snpedia.com/index.php?title=Rs2975766 reference = Chr8 illumina rs2976392 143759934..143759934 "rs2976392 and diffuse-type gastric cancer (allele-specific odds ratio (OR) = 1.62, 95% CI = 1.38-1.8..." http://www.snpedia.com/index.php?title=Rs2976392 reference = Chr8 snp rs2977838 145611219..145611219 "" http://www.snpedia.com/index.php?title=Rs2977838 reference = Chr10 snp rs2981578 123330301..123330301 "rs2981578 is a SNP within intron 2 of the FGFR2 gene, as part of a haplotype associated with increas..." http://www.snpedia.com/index.php?title=Rs2981578 reference = Chr10 illumina rs2981579 123327325..123327325 "This SNP is basically a proxy for SNP rs1219648, which represents the SNP in the FGFR2 gene with the..." http://www.snpedia.com/index.php?title=Rs2981579 reference = Chr10 both rs2981582 123342307..123342307 "rs2981582, a SNP associated with the FGFR2 gene, was one of the four strongest associating SNPs foun..." http://www.snpedia.com/index.php?title=Rs2981582 reference = Chr10 snp rs2986017 105208242..105208242 "rs2986017, also known as L86P, is a SNP in the CALHM1 gene. This gene encodes a multipass transmembr..." http://www.snpedia.com/index.php?title=Rs2986017 reference = Chr14 affy rs2987983 63833406..63833406 "In one large Swedish study, men with one or two rs2987983(C) alleles were reported to be at somewhat..." http://www.snpedia.com/index.php?title=Rs2987983 reference = Chr9 illumina rs2989727 136951519..136951519 "the A allele rs2989727 was significantly increased in RA patients (67%) compared with controls (60%)..." http://www.snpedia.com/index.php?title=Rs2989727 reference = Chr5 both rs299290 162835094..162835094 "[http://cancergenetics.wordpress.com/2007/10/13/exciting-discoveries-of-2007-breast-cancer/ cancerge..." http://www.snpedia.com/index.php?title=Rs299290 reference = Chr1 affy rs3008621 220870669..220870669 "" http://www.snpedia.com/index.php?title=Rs3008621 reference = Chr10 snp rs3013236 124320417..124320417 "" http://www.snpedia.com/index.php?title=Rs3013236 reference = Chr5 illumina rs30168 13772089..13772089 "" http://www.snpedia.com/index.php?title=Rs30168 reference = Chr18 illumina rs3018362 58233073..58233073 "rs3018362 increases susceptibility to Osteoporotic fractures for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs3018362 reference = Chr5 illumina rs30187 96150086..96150086 "rs30187 is one of several SNPs in the ARTS1 gene that has been shown in a large (over 1,000 Caucasia..." http://www.snpedia.com/index.php?title=Rs30187 reference = Chr6 both rs3020314 152312365..152312365 "Associated with (reduced) risk for follicular lymphoma. Based on studying ~1,300 patients in 2 popul..." http://www.snpedia.com/index.php?title=Rs3020314 reference = Chr14 snp rs3021119 23637338..23637338 "" http://www.snpedia.com/index.php?title=Rs3021119 reference = Chr1 snp rs3024492 205010735..205010735 "Dust mite exposure modifies the effect of functional IL10 polymorphisms on allergy and asthma exacer..." http://www.snpedia.com/index.php?title=Rs3024492 reference = Chr1 illumina rs3024496 205008487..205008487 "Dust mite exposure modifies the effect of functional IL10 polymorphisms on allergy and asthma exacer..." http://www.snpedia.com/index.php?title=Rs3024496 reference = Chr2 snp rs3024791 85749215..85749215 "In a study of 389 non-Hispanic Caucasian patients with chronic obstructive pulmonary disease (COPD),..." http://www.snpedia.com/index.php?title=Rs3024791 reference = Chr6 snp rs3025039 43860514..43860514 "rs3025039, also known as the +936C/T SNP in the VEGFA gene, has been associated with age-related mac..." http://www.snpedia.com/index.php?title=Rs3025039 reference = Chr11 snp rs3025058 102221162..102221162 "SNP rs3025058 was first described in 1995 as a variant upstream of, and influencing the regulation o..." http://www.snpedia.com/index.php?title=Rs3025058 reference = Chr10 illumina rs3026785 42945692..42945692 "Associated with protection from Hirschsprung disease See OMIM [http://www.ncbi.nlm.nih.gov/entrez/di..." http://www.snpedia.com/index.php?title=Rs3026785 reference = ChrX both rs3027898 152929084..152929084 "The A->C rs3027898 polymorphism of the IRAK1 gene was significantly associated with atherothrombotic..." http://www.snpedia.com/index.php?title=Rs3027898 reference = Chr5 illumina rs30740 135354489..135354489 "Visceral leishmaniasis (VL) caused by Leishmania chagasi is endemic to northeast Brazil. A positive ..." http://www.snpedia.com/index.php?title=Rs30740 reference = Chr5 both rs30832 149341070..149341070 "" http://www.snpedia.com/index.php?title=Rs30832 reference = Chr2 affy rs3087243 204447164..204447164 "The rs3087243 SNP is also known in the literature as the CT60 G>A or the +6230G>A polymorphism, and ..." http://www.snpedia.com/index.php?title=Rs3087243 reference = Chr15 snp rs3087454 30108259..30108259 "associated with specific patterns of brain activity. rs3087454 rs1355920 rs7520974 rs885834" http://www.snpedia.com/index.php?title=Rs3087454 reference = Chr16 snp rs3087456 10878403..10878403 "This snp has been linked to increased risk of [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubm..." http://www.snpedia.com/index.php?title=Rs3087456 reference = Chr1 snp rs3091244 157951289..157951289 "This is a triallelic SNP - note that the sidebar (currently) only shows 3 of the 6 possible genotype..." http://www.snpedia.com/index.php?title=Rs3091244 reference = Chr22 snp rs3091367 36557767..36557767 "alcoholism rs3091367" http://www.snpedia.com/index.php?title=Rs3091367 reference = Chr11 snp rs3092856 107664942..107664942 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs3092856 reference = Chr11 illumina rs3092857 107648509..107648509 "[omim:B-CELL NON-HODGKIN LYMPHOMA, SOMATIC]" http://www.snpedia.com/index.php?title=Rs3092857 reference = Chr13 snp rs3092891 47851731..47851731 "[omim:RETINOBLASTOMA]" http://www.snpedia.com/index.php?title=Rs3092891 reference = Chr1 illumina rs3093059 157951760..157951760 "Association study of CRP gene polymorphisms with serum CRP level and cardiovascular risk rs3093059 r..." http://www.snpedia.com/index.php?title=Rs3093059 reference = Chr1 snp rs3093061 157951606..157951606 "rs3093061 is a SNP in the promoter of the C-reactive protein CRP gene. rs3093061 associated with SL..." http://www.snpedia.com/index.php?title=Rs3093061 reference = Chr5 illumina rs3095870 172596060..172596060 "rs3095870 is a SNP in the promoter region of the NKX2.5 gene; it is also known as -1192C>T. rs309587..." http://www.snpedia.com/index.php?title=Rs3095870 reference = Chr3 illumina rs310762 12199151..12199151 "rs795009 and rs310762 have been linked to schizophrenia" http://www.snpedia.com/index.php?title=Rs310762 reference = Chr10 both rs3118470 6141719..6141719 "rs3118470 increases susceptibility to Type I Diabetes 1.28 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs3118470 reference = Chr6 illumina rs3129763 32698903..32698903 "Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature] Graves' disease or m..." http://www.snpedia.com/index.php?title=Rs3129763 reference = Chr6 both rs3129934 32444165..32444165 "associated with type-1 diabetes" http://www.snpedia.com/index.php?title=Rs3129934 reference = Chr6 illumina rs3130340 32352605..32352605 "rs3130340 increases susceptibility to Bone mineral density variations, lower for carriers of the T a..." http://www.snpedia.com/index.php?title=Rs3130340 reference = Chr9 snp rs3132293 136465643..136465643 "A screen of SNPs in the RXRA gene in 405 Alzheimer's disease patients (mean age 74 +/- 9 years) sugg..." http://www.snpedia.com/index.php?title=Rs3132293 reference = Chr6 illumina rs3132453 31712023..31712023 "rs3132453, a SNP in the BAT2 gene also known as V1883L, is associated with reduced risk for developi..." http://www.snpedia.com/index.php?title=Rs3132453 reference = Chr6 illumina rs3135388 32521029..32521029 "Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature] rs3135388 is highly ..." http://www.snpedia.com/index.php?title=Rs3135388 reference = Chr11 snp rs3135506 116167617..116167617 "also known as S19W discussed in , however the snp which prevents [http://www.medicalnewstoday.com/me..." http://www.snpedia.com/index.php?title=Rs3135506 reference = Chr6 snp rs3176336 36756794..36756794 "rs3176336 shows an association with breast cancer in a British study involving ~2300 patients. The o..." http://www.snpedia.com/index.php?title=Rs3176336 reference = Chr19 illumina rs3177751 56542102..56542102 "" http://www.snpedia.com/index.php?title=Rs3177751 reference = Chr20 illumina rs3178250 6708201..6708201 "rs3178250(C;C)protected against otosclerosis (combined populations: p = 2.2 x 10(-4); OR = 2.027; 95..." http://www.snpedia.com/index.php?title=Rs3178250 reference = Chr1 snp rs3180383 23995279..23995279 "[omim:GALACTOSE EPIMERASE DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs3180383 reference = Chr12 illumina rs3184504 110368991..110368991 "rs3184504 is a nonsynonymous SNP in the SH2B3 gene, and it is also known as R262W. In a recent (2008..." http://www.snpedia.com/index.php?title=Rs3184504 reference = Chr2 snp rs3188996 113709544..113709544 "[omim:PAX8 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs3188996 reference = Chr5 illumina rs3194051 35912031..35912031 "rs3194051, one of several SNPs in the IL7R gene, has been reported in a large study to be associated..." http://www.snpedia.com/index.php?title=Rs3194051 reference = Chr5 snp rs3195676 34043857..34043857 "" http://www.snpedia.com/index.php?title=Rs3195676 reference = Chr3 illumina rs3197999 49696536..49696536 "[http://spittoon.23andme.com/2008/06/30/snpwatch-number-of-snps-associated-with-crohn%E2%80%99s-dise..." http://www.snpedia.com/index.php?title=Rs3197999 reference = Chr9 both rs3204145 110691441..110691441 "" http://www.snpedia.com/index.php?title=Rs3204145 reference = Chr7 illumina rs3211938 80138385..80138385 "2020 African Americans. rs3211938, previously shown to influence malaria susceptibility, is document..." http://www.snpedia.com/index.php?title=Rs3211938 reference = Chr5 illumina rs3212227 158675528..158675528 "IL12B gene SNP, part of a haplotype with rs6887695 associated with psoriasis." http://www.snpedia.com/index.php?title=Rs3212227 reference = Chr6 snp rs3212236 24756434..24756434 "The more common allele of rs3212236 has been linked to increased risk for developmental dyslexia in ..." http://www.snpedia.com/index.php?title=Rs3212236 reference = ChrY snp rs3212287 20359276..20359276 "" http://www.snpedia.com/index.php?title=Rs3212287 reference = ChrY snp rs3212290 20397920..20397920 "" http://www.snpedia.com/index.php?title=Rs3212290 reference = ChrNone snp rs3212291 13360920..13360920 "" http://www.snpedia.com/index.php?title=Rs3212291 reference = ChrNone snp rs3212292 13360932..13360932 "" http://www.snpedia.com/index.php?title=Rs3212292 reference = ChrNone affy rs3212294 13540044..13540044 "" http://www.snpedia.com/index.php?title=Rs3212294 reference = Chr5 snp rs3213119 158676366..158676366 "" http://www.snpedia.com/index.php?title=Rs3213119 reference = Chr9 snp rs3218005 21990247..21990247 "rs3218005 shows an association with breast cancer in a British study involving ~2300 patients. The o..." http://www.snpedia.com/index.php?title=Rs3218005 reference = Chr7 illumina rs3218536 151976940..151976940 "rs3218536, a relatively rare SNP also known as Arg188His located in the DNA-repair gene XRCC2, is as..." http://www.snpedia.com/index.php?title=Rs3218536 reference = Chr11 snp rs3218695 107634988..107634988 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs3218695 reference = ChrNone snp rs3218707 107619937..107619937 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs3218707 reference = Chr14 snp rs3218713 22970517..22970517 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1]" http://www.snpedia.com/index.php?title=Rs3218713 reference = Chr14 snp rs3218714 22968328..22968328 "[omim:CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1]" http://www.snpedia.com/index.php?title=Rs3218714 reference = ChrNone snp rs3219018 159817466..159817466 "[omim:SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs3219018 reference = Chr2 illumina rs3219156 202333860..202333860 "" http://www.snpedia.com/index.php?title=Rs3219156 reference = Chr1 illumina rs324420 46643348..46643348 "[omim:DRUG ADDICTION, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs324420 reference = Chr7 snp rs324640 136339536..136339536 "and or this [http://www.tweelingenregister.org/nederlands/verslaggeving/congresbezoek/Gosso_ESHG_20..." http://www.snpedia.com/index.php?title=Rs324640 reference = Chr7 affy rs324650 136344201..136344201 "Category:interesting This snp (and perhaps its neighbors) may influence intelligence and alcohol dep..." http://www.snpedia.com/index.php?title=Rs324650 reference = Chr7 affy rs324981 34784638..34784638 "asthma related influences sleep patterns [http://originsgenomeresources.net/musings/?p=62] [omim:AS..." http://www.snpedia.com/index.php?title=Rs324981 reference = Chr8 affy rs326 19863719..19863719 "The (A) allele of rs326 was associated with risk for lower high-density lipoprotein (HDL) cholestero..." http://www.snpedia.com/index.php?title=Rs326 reference = Chr5 snp rs326118 7921543..7921543 "rs326118 is reported to represent a risk factor for abdominal aortic aneurysm (AAA), with odds ratio..." http://www.snpedia.com/index.php?title=Rs326118 reference = Chr2 snp rs3313172 54277421..54277421 "rs3313172, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs3313172 reference = Chr7 snp rs332 116986883..116986883 "This variation, when inherited from both parents (giving rise to the homozygous rs332(-;-) genotype)..." http://www.snpedia.com/index.php?title=Rs332 reference = Chr3 snp rs333 46389951..46389951 "The chemokine receptor gene CCR5 plays an important role in many immune-related processes. rs333, th..." http://www.snpedia.com/index.php?title=Rs333 reference = Chr1 snp rs333662 59516502..59516502 "rs333662 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have be..." http://www.snpedia.com/index.php?title=Rs333662 reference = Chr11 snp rs334 5204808..5204808 "The most common allele of rs334 is (A), encoding the Hb A form of (adult) hemoglobin. rs334(T) encod..." http://www.snpedia.com/index.php?title=Rs334 reference = Chr9 illumina rs334348 100952292..100952292 "appears relevant to colon cancer rs334348, rs334349 and rs1590 (in total linkage disequilibrium with..." http://www.snpedia.com/index.php?title=Rs334348 reference = Chr9 affy rs334349 100954208..100954208 "appears relevant to colon cancer rs334348, rs334349 and rs1590 (in total linkage disequilibrium with..." http://www.snpedia.com/index.php?title=Rs334349 reference = Chr3 snp rs334558 121295972..121295972 "Although not associated with increased risk for developing bipolar disorder, amongst those with it, ..." http://www.snpedia.com/index.php?title=Rs334558 reference = ChrX illumina rs33910054 48948686..48948686 "" http://www.snpedia.com/index.php?title=Rs33910054 reference = Chr3 snp rs33917740 168989631..168989631 "" http://www.snpedia.com/index.php?title=Rs33917740 reference = Chr18 snp rs33926449 55177341..55177341 "" http://www.snpedia.com/index.php?title=Rs33926449 reference = Chr22 snp rs33928909 24616738..24616738 "" http://www.snpedia.com/index.php?title=Rs33928909 reference = Chr15 snp rs33931006 38702123..38702123 "" http://www.snpedia.com/index.php?title=Rs33931006 reference = Chr5 both rs339445 13997512..13997512 "" http://www.snpedia.com/index.php?title=Rs339445 reference = Chr2 snp rs33958626 110316315..110316315 "" http://www.snpedia.com/index.php?title=Rs33958626 reference = Chr1 snp rs33981382 17541475..17541475 "" http://www.snpedia.com/index.php?title=Rs33981382 reference = Chr3 snp rs33988592 122898300..122898300 "" http://www.snpedia.com/index.php?title=Rs33988592 reference = ChrNone illumina rs34043621 12996675..12996675 "" http://www.snpedia.com/index.php?title=Rs34043621 reference = ChrY snp rs34078768 20328251..20328251 "" http://www.snpedia.com/index.php?title=Rs34078768 reference = Chr2 snp rs34116584 241456987..241456987 "" http://www.snpedia.com/index.php?title=Rs34116584 reference = ChrY illumina rs34126399 21431366..21431366 "[http://spittoon.23andme.com/2008/07/25/the-origin-of-farming-in-europe-a-view-from-the-y-chromosome..." http://www.snpedia.com/index.php?title=Rs34126399 reference = Chr12 snp rs34187924 50967675..50967675 "" http://www.snpedia.com/index.php?title=Rs34187924 reference = Chr1 snp rs34188929 16226981..16226981 "" http://www.snpedia.com/index.php?title=Rs34188929 reference = Chr16 snp rs34197769 2084177..2084177 "" http://www.snpedia.com/index.php?title=Rs34197769 reference = Chr17 snp rs34210653 4482063..4482063 "rs34210653 is a SNP in the ALOX15 gene, either encoding a threonine or a methionine at position 560 ..." http://www.snpedia.com/index.php?title=Rs34210653 reference = Chr12 snp rs34230288 5973355..5973355 "" http://www.snpedia.com/index.php?title=Rs34230288 reference = ChrNone snp rs34248257 13378896..13378896 "" http://www.snpedia.com/index.php?title=Rs34248257 reference = Chr1 snp rs34248917 5873600..5873600 "" http://www.snpedia.com/index.php?title=Rs34248917 reference = Chr16 snp rs34258285 8814415..8814415 "" http://www.snpedia.com/index.php?title=Rs34258285 reference = ChrY illumina rs34276300 20616699..20616699 "[http://www.jogg.info/41/Turner.htm] Since R1b1c is very common, the first interesting discovery inv..." http://www.snpedia.com/index.php?title=Rs34276300 reference = ChrY illumina rs34289137 20210837..20210837 "" http://www.snpedia.com/index.php?title=Rs34289137 reference = Chr12 illumina rs34330 12761962..12761962 "Category:interesting rs34330 shows an association with breast cancer in a British study involving ~2..." http://www.snpedia.com/index.php?title=Rs34330 reference = Chr17 snp rs34424835 39783075..39783075 "Associated with risk of amyotrophic lateral sclerosis (ALS) in two European populations" http://www.snpedia.com/index.php?title=Rs34424835 reference = ChrNone illumina rs34442126 13431977..13431977 "" http://www.snpedia.com/index.php?title=Rs34442126 reference = Chr5 snp rs34482796 147457744..147457744 "" http://www.snpedia.com/index.php?title=Rs34482796 reference = Chr2 snp rs34505188 227836812..227836812 "" http://www.snpedia.com/index.php?title=Rs34505188 reference = Chr15 snp rs34516635 97269499..97269499 "rs34516635 is one of a small number of (rare) SNPs in the IGF1R gene found in a study of 384 Ashkena..." http://www.snpedia.com/index.php?title=Rs34516635 reference = Chr7 snp rs34545616 128639103..128639103 "" http://www.snpedia.com/index.php?title=Rs34545616 reference = Chr7 snp rs34585297 137920110..137920110 "" http://www.snpedia.com/index.php?title=Rs34585297 reference = Chr20 snp rs34604265 57329474..57329474 "" http://www.snpedia.com/index.php?title=Rs34604265 reference = Chr5 illumina rs34677 34034525..34034525 "" http://www.snpedia.com/index.php?title=Rs34677 reference = Chr17 snp rs34693726 10253197..10253197 "" http://www.snpedia.com/index.php?title=Rs34693726 reference = Chr17 snp rs34712518 73632626..73632626 "" http://www.snpedia.com/index.php?title=Rs34712518 reference = Chr8 snp rs34727075 41669540..41669540 "" http://www.snpedia.com/index.php?title=Rs34727075 reference = Chr14 snp rs34728766 104680445..104680445 "" http://www.snpedia.com/index.php?title=Rs34728766 reference = Chr6 snp rs34738426 7526746..7526746 "" http://www.snpedia.com/index.php?title=Rs34738426 reference = Chr4 snp rs34745240 187359326..187359326 "" http://www.snpedia.com/index.php?title=Rs34745240 reference = Chr2 snp rs34815109 234333619..234333619 "rs34815109 is one of four SNPs all describing an insertion/deletion polymorphism in the promoter reg..." http://www.snpedia.com/index.php?title=Rs34815109 reference = Chr5 snp rs34838342 42601743..42601743 "" http://www.snpedia.com/index.php?title=Rs34838342 reference = Chr19 snp rs34844088 18043997..18043997 "" http://www.snpedia.com/index.php?title=Rs34844088 reference = Chr7 snp rs34857375 100556427..100556427 "This SNP is equivalent to, and therefore please go to, rs1799889 for related information." http://www.snpedia.com/index.php?title=Rs34857375 reference = Chr5 affy rs348594 40359695..40359695 "rs348594 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's d..." http://www.snpedia.com/index.php?title=Rs348594 reference = Chr5 illumina rs348601 40355763..40355763 "rs348601 increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele" http://www.snpedia.com/index.php?title=Rs348601 reference = Chr15 snp rs34908405 63276933..63276933 "" http://www.snpedia.com/index.php?title=Rs34908405 reference = Chr3 snp rs34958067 48430159..48430159 "" http://www.snpedia.com/index.php?title=Rs34958067 reference = Chr1 snp rs34967813 235908013..235908013 "" http://www.snpedia.com/index.php?title=Rs34967813 reference = Chr2 snp rs34983651 234333618..234333618 "rs34983651 is one of four SNPs all describing an insertion/deletion polymorphism in the promoter reg..." http://www.snpedia.com/index.php?title=Rs34983651 reference = Chr11 snp rs35068180 102221157..102221157 "*see rs3025058, which covers the same polymorphism" http://www.snpedia.com/index.php?title=Rs35068180 reference = Chr1 snp rs35095275 153451040..153451040 "rs35095275, a SNP causing an amino acid change in the GBA gene, has been determined to be the most c..." http://www.snpedia.com/index.php?title=Rs35095275 reference = Chr19 snp rs35136575 50131003..50131003 "Lower plasma LDL-C was observed with the rare allele. Plasma apoE level was strongly associated with..." http://www.snpedia.com/index.php?title=Rs35136575 reference = Chr9 snp rs35142681 112489310..112489310 "" http://www.snpedia.com/index.php?title=Rs35142681 reference = Chr5 snp rs351855 176452849..176452849 "rs351855, a SNP in the fibroblast growth factor receptor 4 (FGFR4) gene, is also known as the Gly388..." http://www.snpedia.com/index.php?title=Rs351855 reference = Chr8 affy rs352203 28450620..28450620 "[http://7thspace.com/headlines/290001/the_frizzled_3_gene_is_associated_with_methamphetamine_psychos..." http://www.snpedia.com/index.php?title=Rs352203 reference = ChrNone illumina rs35284970 2794854..2794854 "" http://www.snpedia.com/index.php?title=Rs35284970 reference = Chr2 snp rs35297901 71644763..71644763 "" http://www.snpedia.com/index.php?title=Rs35297901 reference = Chr8 snp rs35301433 133952825..133952825 "" http://www.snpedia.com/index.php?title=Rs35301433 reference = Chr7 snp rs35332062 72649978..72649978 "" http://www.snpedia.com/index.php?title=Rs35332062 reference = Chr1 snp rs35369693 204391258..204391258 "The very common allele of rs35369693 was observed to be associated with child-onset mood disorders (..." http://www.snpedia.com/index.php?title=Rs35369693 reference = Chr10 snp rs35441642 15016733..15016733 "" http://www.snpedia.com/index.php?title=Rs35441642 reference = Chr6 snp rs35445429 32084894..32084894 "" http://www.snpedia.com/index.php?title=Rs35445429 reference = Chr6 snp rs35445598 73000226..73000226 "" http://www.snpedia.com/index.php?title=Rs35445598 reference = Chr5 snp rs35515200 176764772..176764772 "" http://www.snpedia.com/index.php?title=Rs35515200 reference = Chr2 snp rs35600288 234333625..234333625 "rs35600288 is one of four SNPs all describing an insertion/deletion polymorphism in the promoter reg..." http://www.snpedia.com/index.php?title=Rs35600288 reference = Chr4 snp rs356219 90856624..90856624 "rs356219, a tagging SNP in the SNCA gene for a Parkinson's disease associated haplotype, predicts th..." http://www.snpedia.com/index.php?title=Rs356219 reference = Chr3 illumina rs35623035 48605256..48605256 "" http://www.snpedia.com/index.php?title=Rs35623035 reference = Chr1 snp rs35669711 22051831..22051831 "" http://www.snpedia.com/index.php?title=Rs35669711 reference = Chr8 snp rs35753505 31593683..31593683 "[http://originsgenomeresources.net/musings/?p=164 blog] rs35753505(C;C) correlates with frontal brai..." http://www.snpedia.com/index.php?title=Rs35753505 reference = Chr9 snp rs35804026 76542160..76542160 "" http://www.snpedia.com/index.php?title=Rs35804026 reference = Chr1 snp rs35856562 184418013..184418013 "" http://www.snpedia.com/index.php?title=Rs35856562 reference = Chr4 snp rs35859249 37580484..37580484 "Also known as the R125W variant, rs35859249 is a SNP in the TBC1D1 gene that has been associated wit..." http://www.snpedia.com/index.php?title=Rs35859249 reference = Chr10 affy rs35866326 58986929..58986929 "rs35866326 increases susceptibility to Parkinson's disease 1.88 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs35866326 reference = Chr3 both rs358806 55288440..55288440 "rs358806 has been reported in a large study to be associated with type-2 diabetes. The risk allele (..." http://www.snpedia.com/index.php?title=Rs358806 reference = Chr20 snp rs35908728 60921750..60921750 "This SNP currently serves only as a marker for a SNP known as Arg103Trp that lacks an rs# in dbSNP, ..." http://www.snpedia.com/index.php?title=Rs35908728 reference = Chr17 snp rs35952774 10248380..10248380 "" http://www.snpedia.com/index.php?title=Rs35952774 reference = Chr6 snp rs36007903 32084904..32084904 "" http://www.snpedia.com/index.php?title=Rs36007903 reference = Chr19 snp rs36070283 18737258..18737258 "" http://www.snpedia.com/index.php?title=Rs36070283 reference = Chr2 snp rs36089250 175752152..175752152 "" http://www.snpedia.com/index.php?title=Rs36089250 reference = Chr6 snp rs361525 31651080..31651080 "rs361525 is also known as the TNF -238 SNP, and occasionally the rs361525(A) allele is referred to a..." http://www.snpedia.com/index.php?title=Rs361525 reference = Chr7 snp rs362691 103038397..103038397 "" http://www.snpedia.com/index.php?title=Rs362691 reference = Chr20 illumina rs363039 10168496..10168496 "This is one of four SNPs in the first intron of the SNAP25 gene that have been correlated with incre..." http://www.snpedia.com/index.php?title=Rs363039 reference = Chr20 illumina rs363043 10174146..10174146 "This is one of four SNPs in the first intron of the SNAP25 gene that have been correlated with incre..." http://www.snpedia.com/index.php?title=Rs363043 reference = Chr20 affy rs363050 10182257..10182257 "This is one of four SNPs in the first intron of the SNAP25 gene that have been correlated with incre..." http://www.snpedia.com/index.php?title=Rs363050 reference = Chr19 illumina rs36686 17783795..17783795 "rs36686, a SNP in the B3GNT3 gene also known as H328R, is associated with reduced risk for developin..." http://www.snpedia.com/index.php?title=Rs36686 reference = Chr5 snp rs3729960 55299910..55299910 "" http://www.snpedia.com/index.php?title=Rs3729960 reference = Chr9 illumina rs3731239 21964218..21964218 "rs3731239 shows a slight protective association against breast cancer in a British study involving ~..." http://www.snpedia.com/index.php?title=Rs3731239 reference = Chr10 snp rs3731566 111876079..111876079 "rs3731566 is a SNP in the adducin 3 ADD3 gene. This variation on its own has not been linked to hype..." http://www.snpedia.com/index.php?title=Rs3731566 reference = Chr2 illumina rs3731824 85941822..85941822 "" http://www.snpedia.com/index.php?title=Rs3731824 reference = Chr3 illumina rs3732379 39282260..39282260 "[omim:HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RAPID PROGRESSION TO AIDS]" http://www.snpedia.com/index.php?title=Rs3732379 reference = Chr4 illumina rs3733197 103058310..103058310 "rs17266594 rs10516487 rs3733197 gene associated with systemic lupus erythematosus." http://www.snpedia.com/index.php?title=Rs3733197 reference = Chr5 illumina rs3733890 78457715..78457715 "Variant BHMT allele may increase risk for neural tube defects, apparently only in folate rich enviro..." http://www.snpedia.com/index.php?title=Rs3733890 reference = Chr5 illumina rs3734110 13754536..13754536 "" http://www.snpedia.com/index.php?title=Rs3734110 reference = Chr16 illumina rs373496 11967664..11967664 "" http://www.snpedia.com/index.php?title=Rs373496 reference = Chr8 both rs3735972 87657314..87657314 "" http://www.snpedia.com/index.php?title=Rs3735972 reference = Chr11 both rs3736228 67957871..67957871 "rs3736228 is a SNP in the LRP5 gene that is also known as Ala1330Val; the more common (C) allele enc..." http://www.snpedia.com/index.php?title=Rs3736228 reference = Chr1 illumina rs3736360 22022707..22022707 "" http://www.snpedia.com/index.php?title=Rs3736360 reference = Chr1 snp rs3737296 218892146..218892146 "Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a re..." http://www.snpedia.com/index.php?title=Rs3737296 reference = Chr1 illumina rs3737787 159276147..159276147 "contributes to high serum lipid levels in Dutch familial combined hyperlipidemia families and U.S. w..." http://www.snpedia.com/index.php?title=Rs3737787 reference = Chr1 illumina rs3737964 11789631..11789631 "Associated with lean body mass but not fat body mass in a study of ~1,800 Caucasians" http://www.snpedia.com/index.php?title=Rs3737964 reference = Chr1 illumina rs3738401 229896918..229896918 "rs3738401 is a SNP in the DISC1 gene, known as R264Q. Associated with schizophrenia 13 single-nucle..." http://www.snpedia.com/index.php?title=Rs3738401 reference = Chr1 illumina rs3738579 180822659..180822659 "rs3738579 represents a SNP in the 5' UTR region upstream of the RNASEL gene. A study of patients dia..." http://www.snpedia.com/index.php?title=Rs3738579 reference = Chr2 illumina rs3738919 187229505..187229505 "rs3738919, a SNP located in the ITGAV gene, was identified in a European study to be associated with..." http://www.snpedia.com/index.php?title=Rs3738919 reference = Chr10 illumina rs3740057 101648575..101648575 "rs3740057 is one of 2 SNPs in the DNMBP gene that has been associated with increased risk for late-o..." http://www.snpedia.com/index.php?title=Rs3740057 reference = Chr10 snp rs3740058 101645972..101645972 "rs3740058 increases susceptibility to Alzheimer's disease, late-onset 1.64 times for heterozygotes (..." http://www.snpedia.com/index.php?title=Rs3740058 reference = Chr10 snp rs3740066 101594197..101594197 "rs3740066, a SNP in the ABCC2 gene, is reported to be associated with a higher risk of developing in..." http://www.snpedia.com/index.php?title=Rs3740066 reference = Chr10 snp rs3740129 73437865..73437865 "" http://www.snpedia.com/index.php?title=Rs3740129 reference = Chr11 illumina rs3740878 44214378..44214378 "rs3740878 increases susceptibility to Type II Diabetes 1.26 times for heterozygotes (AG) and 1.46 ti..." http://www.snpedia.com/index.php?title=Rs3740878 reference = Chr11 both rs3740955 36552176..36552176 "" http://www.snpedia.com/index.php?title=Rs3740955 reference = Chr11 affy rs3741208 2126350..2126350 "associated with type-1 diabetes" http://www.snpedia.com/index.php?title=Rs3741208 reference = Chr12 both rs3741981 111833253..111833253 "Was investigated for a diabetes association, but seemed to have none. suggests it or a neighbor may..." http://www.snpedia.com/index.php?title=Rs3741981 reference = Chr16 snp rs3743930 3244627..3244627 "[omim:FAMILIAL MEDITERRANEAN FEVER]" http://www.snpedia.com/index.php?title=Rs3743930 reference = Chr20 snp rs3746444 33041912..33041912 "microRNA 1,009 breast cancer cases and 1,093 controls in a population of Chinese women *rs3746444 in..." http://www.snpedia.com/index.php?title=Rs3746444 reference = Chr6 illumina rs3748079 33696125..33696125 "rs3748079 is a SNP in the promoter region of the ITPR3 gene; it is also known as -1990C>T. rs3748079..." http://www.snpedia.com/index.php?title=Rs3748079 reference = Chr9 illumina rs3750344 100380137..100380137 "Associated with Nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs3750344 reference = Chr10 illumina rs3750861 3814433..3814433 "rs10508266 and rs3750861 shows significant association with lung cancer risk rs3750861 affects expr..." http://www.snpedia.com/index.php?title=Rs3750861 reference = Chr16 illumina rs3751812 52375961..52375961 "Within the FTO gene, many SNPs appear to be co-inherited. The SNP showing the strongest association ..." http://www.snpedia.com/index.php?title=Rs3751812 reference = Chr18 snp rs3752095 27188679..27188679 "" http://www.snpedia.com/index.php?title=Rs3752095 reference = Chr1 illumina rs3753394 194887540..194887540 "linked to blindness in old age rs3753394 carries a significantly increased risk for exudative AMD. ..." http://www.snpedia.com/index.php?title=Rs3753394 reference = Chr2 illumina rs3755351 70828398..70828398 "rs3755351, a SNP in the ADD2 gene, was associated with risk for hypertension in a study involving 1,..." http://www.snpedia.com/index.php?title=Rs3755351 reference = Chr5 both rs3756450 1501148..1501148 "schizophrenia p = 0.035" http://www.snpedia.com/index.php?title=Rs3756450 reference = Chr10 illumina rs3758391 69313348..69313348 "rs3758391, a SNP in the SIRT1 gene, has been reported to potentially have some role in either longev..." http://www.snpedia.com/index.php?title=Rs3758391 reference = Chr10 illumina rs3758549 103994185..103994185 "CC linked to parkinson's disease We provide evidence for a novel, strong and reproducible associati..." http://www.snpedia.com/index.php?title=Rs3758549 reference = Chr17 snp rs3760468 46585490..46585490 "breast cancer strong linkage disequilibrium for rs16949646 rs2302254 and rs3760468" http://www.snpedia.com/index.php?title=Rs3760468 reference = Chr17 illumina rs3760511 33180426..33180426 "rs3760511 increases susceptibility to Prostate cancer 1.16 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs3760511 reference = Chr20 both rs3761218 3724175..3724175 "rs3761218 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs3761218 reference = Chr22 illumina rs3761418 21851094..21851094 "rs3761418, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for depre..." http://www.snpedia.com/index.php?title=Rs3761418 reference = Chr9 illumina rs3761847 122730060..122730060 "rs3761847, a SNP located between two genes associated with chronic inflammation (TRAF1 and C5), is a..." http://www.snpedia.com/index.php?title=Rs3761847 reference = Chr15 both rs3764220 49759350..49759350 "This SNP in the SCG3 gene was significantly associated with an obesity phenotype. Two other SNPs, rs..." http://www.snpedia.com/index.php?title=Rs3764220 reference = Chr7 snp rs3765187 79930654..79930654 "[omim:PLATELET GLYCOPROTEIN IV DEFICIENCY]" http://www.snpedia.com/index.php?title=Rs3765187 reference = Chr1 both rs3765598 114195986..114195986 "rs3765598 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumato..." http://www.snpedia.com/index.php?title=Rs3765598 reference = Chr2 illumina rs3770748 37449029..37449029 "rs3770748, a SNP in an intron of the QPCT gene, was studied in a population of ~200 Chinese osteopor..." http://www.snpedia.com/index.php?title=Rs3770748 reference = Chr2 illumina rs3771150 102427283..102427283 "This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients." http://www.snpedia.com/index.php?title=Rs3771150 reference = Chr3 both rs3772534 106903724..106903724 "One report based on a study of 480 Danish families indicated that the rs3772534 SNP in the CBLB gene..." http://www.snpedia.com/index.php?title=Rs3772534 reference = Chr4 both rs3775291 187241068..187241068 "rs3775291 is a SNP in the TLR3 gene associated with an amino acid change in the corresponding protei..." http://www.snpedia.com/index.php?title=Rs3775291 reference = Chr5 illumina rs3777134 147478212..147478212 "" http://www.snpedia.com/index.php?title=Rs3777134 reference = Chr8 both rs3779748 72410728..72410728 "rs3779748 in EYA1, was significantly associated with kidney disease (odds ratio per each T allele 1...." http://www.snpedia.com/index.php?title=Rs3779748 reference = Chr9 snp rs3780422 100182625..100182625 "Associated with nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjec..." http://www.snpedia.com/index.php?title=Rs3780422 reference = Chr12 snp rs3782206 116229472..116229472 "schizophrenia 1705 Chinese subjects. rs3782206 associated with paranoid schizophrenia" http://www.snpedia.com/index.php?title=Rs3782206 reference = Chr14 snp rs3783799 60988969..60988969 "A common SNP only in Asian populations, this SNP and a close neighbor also in PRKCH gene, rs3783799,..." http://www.snpedia.com/index.php?title=Rs3783799 reference = Chr15 both rs3784709 65859329..65859329 "rs3784709, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of rest..." http://www.snpedia.com/index.php?title=Rs3784709 reference = ChrX affy rs3788853 128698472..128698472 "A form of this snp, located upstream of the XPNPEP2 gene on the X chromosome, may cause susceptibili..." http://www.snpedia.com/index.php?title=Rs3788853 reference = Chr2 both rs3788964 162915726..162915726 "" http://www.snpedia.com/index.php?title=Rs3788964 reference = Chr1 snp rs3789604 114156465..114156465 "rs3789604 is associated with increased susceptibility to rheumatoid arthritis, based on a study of ~..." http://www.snpedia.com/index.php?title=Rs3789604 reference = Chr2 illumina rs3791878 171380437..171380437 "implicated in schizophrenia" http://www.snpedia.com/index.php?title=Rs3791878 reference = Chr2 both rs3792267 241179847..241179847 "summary, indicating a small effect of this SNP, seen only in meta-analyses rs3792267 associated with..." http://www.snpedia.com/index.php?title=Rs3792267 reference = Chr4 snp rs3792683 100729926..100729926 "" http://www.snpedia.com/index.php?title=Rs3792683 reference = Chr5 illumina rs3792876 131665208..131665208 "NOTE: information for rs1050152 was accidentally entered for this SNP, rs3792876. Although the SNPs ..." http://www.snpedia.com/index.php?title=Rs3792876 reference = Chr10 snp rs3793784 50417545..50417545 "rs3793784, a SNP upstream of the ERCC6 DNA repair gene, has been linked independently and in conjunc..." http://www.snpedia.com/index.php?title=Rs3793784 reference = Chr12 illumina rs3794260 107122404..107122404 "rs3794260, a SNP in the KIAA0789 gene, was associated with risk for hypertension in a study involvin..." http://www.snpedia.com/index.php?title=Rs3794260 reference = Chr6 illumina rs3798220 160881127..160881127 "coronary artery disease rs3798220 I4399M Compared with noncarriers, carriers of the 4399M risk allel..." http://www.snpedia.com/index.php?title=Rs3798220 reference = Chr6 illumina rs3800373 35650454..35650454 "rs9296158 rs3800373 rs1360780 rs9470080 linked with the severity of child abuse to predict level of ..." http://www.snpedia.com/index.php?title=Rs3800373 reference = Chr7 illumina rs3800855 157677910..157677910 "" http://www.snpedia.com/index.php?title=Rs3800855 reference = Chr8 illumina rs3802177 118254206..118254206 "rs3802177 replicated as significant for type-2 diabetes risk in 1,900 Japanese patients, with odds r..." http://www.snpedia.com/index.php?title=Rs3802177 reference = Chr11 snp rs3802780 69958640..69958640 "rs3802780 was significantly associated with severe asthma (odds ratio 1.71, CI: 1.20-2.43;, p=0.003)..." http://www.snpedia.com/index.php?title=Rs3802780 reference = Chr11 illumina rs3802842 110676919..110676919 "rs3802842(C) associated with risk of colorectal cancer across a total of 10,638 cases and 10,457. pe..." http://www.snpedia.com/index.php?title=Rs3802842 reference = Chr11 snp rs3802905 124254794..124254794 "rs3802905 has been reported to be a SNP potentially associated with increased risk for autism" http://www.snpedia.com/index.php?title=Rs3802905 reference = Chr3 illumina rs3803 129682070..129682070 "Category:needs help Category:interesting [http://genetics.plosjournals.org/perlserv/?request=get-doc..." http://www.snpedia.com/index.php?title=Rs3803 reference = Chr12 snp rs3803183 46684347..46684347 "" http://www.snpedia.com/index.php?title=Rs3803183 reference = Chr13 snp rs3803185 49103026..49103026 "" http://www.snpedia.com/index.php?title=Rs3803185 reference = Chr14 snp rs3803300 104340824..104340824 "G allele associated with schizophrenia" http://www.snpedia.com/index.php?title=Rs3803300 reference = Chr15 illumina rs3803369 49163121..49163121 "rs3803369 was a significant SNP associated with risk for psoriasis in a large US/UK study." http://www.snpedia.com/index.php?title=Rs3803369 reference = Chr16 both rs3803662 51143842..51143842 "rs3803662, a SNP associated with the TNRC9 gene, was one of the four strongest associating SNPs foun..." http://www.snpedia.com/index.php?title=Rs3803662 reference = Chr1 snp rs380390 194967674..194967674 "linked to blindness in old age rs3753394, rs800292, rs1061147, rs1061170, rs380390, and rs1329428 CF..." http://www.snpedia.com/index.php?title=Rs380390 reference = Chr6 both rs3804505 52411320..52411320 "[omim:MYOCLONIC EPILEPSY, JUVENILE, 1]" http://www.snpedia.com/index.php?title=Rs3804505 reference = Chr1 illumina rs3806265 245652959..245652959 "rs3806265 was associated with juvenile idiopathic arthritis based on a study of 950 Caucasian patien..." http://www.snpedia.com/index.php?title=Rs3806265 reference = Chr7 both rs3807153 138068331..138068331 "[omim:RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE]" http://www.snpedia.com/index.php?title=Rs3807153 reference = Chr7 affy rs3807306 128367916..128367916 "rs4728142, rs3807306 and a 5 bp insertion-deletion linked multiple sclerosis in three populations A..." http://www.snpedia.com/index.php?title=Rs3807306 reference = ChrX affy rs3810682 50670515..50670515 "Associated with ovarian failure" http://www.snpedia.com/index.php?title=Rs3810682 reference = ChrX illumina rs3810710 19285703..19285703 "A (G) form of this SNP, located in exon 9 of the PDHA1 gene, has been observed in patients with pyru..." http://www.snpedia.com/index.php?title=Rs3810710 reference = Chr9 both rs3810936 116592706..116592706 "Associated with increased risk for Crohn's disease in a study of 380 Korean patients." http://www.snpedia.com/index.php?title=Rs3810936 reference = Chr2 illumina rs3811635 112471472..112471472 "" http://www.snpedia.com/index.php?title=Rs3811635 reference = Chr6 illumina rs3812153 80683094..80683094 "" http://www.snpedia.com/index.php?title=Rs3812153 reference = Chr7 snp rs3812316 72658273..72658273 "rs3812316, a SNP in the MLXIPL gene that is also known as G771C or Gln241His, has been observed in a..." http://www.snpedia.com/index.php?title=Rs3812316 reference = Chr2 affy rs3812718 166617790..166617790 "Genetic predictors of the maximum doses patients receive during anti-epileptic drugs carbamazepine a..." http://www.snpedia.com/index.php?title=Rs3812718 reference = Chr10 affy rs3814219 105637085..105637085 "BA baseline flow, rs3814219 (OBFC1, 9.48*10(-7))" http://www.snpedia.com/index.php?title=Rs3814219 reference = Chr4 both rs3816587 25026342..25026342 "rs3816587 has been reported in a large study to be associated with rheumatoid arthritis. The risk al..." http://www.snpedia.com/index.php?title=Rs3816587 reference = Chr15 illumina rs3816800 23476187..23476187 "" http://www.snpedia.com/index.php?title=Rs3816800 reference = Chr4 illumina rs3816873 100723687..100723687 "Also known as I128T MTP rare allele of the MTP I128T polymorphism may be protective against impaired..." http://www.snpedia.com/index.php?title=Rs3816873 reference = Chr11 both rs3817198 1865582..1865582 "rs3817198, a SNP associated with the LSP1 gene, was one of the four strongest associating SNPs found..." http://www.snpedia.com/index.php?title=Rs3817198 reference = Chr1 snp rs381737 153474556..153474556 "[omim:GAUCHER DISEASE, TYPE III]" http://www.snpedia.com/index.php?title=Rs381737 reference = Chr6 illumina rs3817964 32475975..32475975 "This SNP, along with SNPs rs6910071 and rs660895, is a tag SNP for the HLA-DRB1*0401 allele. The HLA..." http://www.snpedia.com/index.php?title=Rs3817964 reference = Chr1 both rs3820129 145558596..145558596 "" http://www.snpedia.com/index.php?title=Rs3820129 reference = Chr11 snp rs3824886 20361189..20361189 "" http://www.snpedia.com/index.php?title=Rs3824886 reference = Chr11 snp rs3824968 120981132..120981132 "Alzheimer's disease rs3824968" http://www.snpedia.com/index.php?title=Rs3824968 reference = Chr15 both rs3825776 56534122..56534122 "rs3825776, a SNP in the region of the LIPC gene on chromosome 15, has been associated with the spora..." http://www.snpedia.com/index.php?title=Rs3825776 reference = Chr15 illumina rs3825942 72006635..72006635 "rs3825942, also known as G153D, a SNP causing an amino acid change in the lysyl oxidase 1 LOXL1 gene..." http://www.snpedia.com/index.php?title=Rs3825942 reference = Chr17 snp rs3826550 36996333..36996333 "" http://www.snpedia.com/index.php?title=Rs3826550 reference = Chr15 both rs3829462 56640371..56640371 "" http://www.snpedia.com/index.php?title=Rs3829462 reference = Chr1 snp rs3831308 199296342..199296342 "[omim:THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs3831308 reference = Chr16 both rs383362 77803321..77803321 "" http://www.snpedia.com/index.php?title=Rs383362 reference = Chr2 snp rs3834129 201805777..201805777 "rs3834129 is a SNP in the CASP8 gene that is also known as the -652 6N ins/del promoter variant. It ..." http://www.snpedia.com/index.php?title=Rs3834129 reference = Chr5 affy rs383830 99976881..99976881 "rs383830 has been reported in a large study to be associated with heart disease, in particular, coro..." http://www.snpedia.com/index.php?title=Rs383830 reference = Chr22 snp rs384262 20342772..20342772 "" http://www.snpedia.com/index.php?title=Rs384262 reference = Chr20 snp rs3843763 43981600..43981600 "The (T) allele of rs3843763 was associated with risk for lower high-density lipoprotein (HDL) choles..." http://www.snpedia.com/index.php?title=Rs3843763 reference = Chr12 illumina rs3847953 110249847..110249847 "rs3847953 and rs933399 associated with bipolar disorder" http://www.snpedia.com/index.php?title=Rs3847953 reference = ChrY both rs3848982 20176596..20176596 "" http://www.snpedia.com/index.php?title=Rs3848982 reference = ChrY both rs3853054 8739843..8739843 "" http://www.snpedia.com/index.php?title=Rs3853054 reference = Chr22 affy rs3859866 24496900..24496900 "" http://www.snpedia.com/index.php?title=Rs3859866 reference = Chr18 affy rs3865418 54155144..54155144 "rs3865418, a SNP in the NEDD4L gene, has been associated with hypertension in a study of Chinese (Ha..." http://www.snpedia.com/index.php?title=Rs3865418 reference = ChrY illumina rs3865828 20553879..20553879 "" http://www.snpedia.com/index.php?title=Rs3865828 reference = Chr12 both rs3887954 51472355..51472355 "" http://www.snpedia.com/index.php?title=Rs3887954 reference = Chr1 snp rs3889728 228915454..228915454 "rs3889728 is a SNP in the AGT gene that, at least when part of a haplotype, has been associated with..." http://www.snpedia.com/index.php?title=Rs3889728 reference = Chr22 snp rs3892097 40854891..40854891 "The normal (or wild type) form of this SNP is a (G). The (A) form disrupts proper mRNA formation, re..." http://www.snpedia.com/index.php?title=Rs3892097 reference = ChrNone snp rs3893 12606579..12606579 "" http://www.snpedia.com/index.php?title=Rs3893 reference = ChrY affy rs3894 17605757..17605757 "" http://www.snpedia.com/index.php?title=Rs3894 reference = ChrNone snp rs3895 2804628..2804628 "" http://www.snpedia.com/index.php?title=Rs3895 reference = ChrY both rs3896 20069334..20069334 "" http://www.snpedia.com/index.php?title=Rs3896 reference = ChrY illumina rs3897 17080420..17080420 "" http://www.snpedia.com/index.php?title=Rs3897 reference = ChrNone snp rs3898 4138217..4138217 "" http://www.snpedia.com/index.php?title=Rs3898 reference = ChrY snp rs3899 7351534..7351534 "" http://www.snpedia.com/index.php?title=Rs3899 reference = ChrY affy rs3900 20189645..20189645 "" http://www.snpedia.com/index.php?title=Rs3900 reference = Chr3 illumina rs3900940 109630418..109630418 "rs3900940 is a SNP in the MYH15 gene. The risk allele in terms of heart disease is rs3900940(C). Thi..." http://www.snpedia.com/index.php?title=Rs3900940 reference = ChrY both rs3901 20182386..20182386 "" http://www.snpedia.com/index.php?title=Rs3901 reference = ChrY both rs3902 20190035..20190035 "" http://www.snpedia.com/index.php?title=Rs3902 reference = ChrY snp rs3903 7643480..7643480 "" http://www.snpedia.com/index.php?title=Rs3903 reference = Chr9 snp rs390312 101125969..101125969 "" http://www.snpedia.com/index.php?title=Rs390312 reference = ChrY affy rs3904 20181486..20181486 "" http://www.snpedia.com/index.php?title=Rs3904 reference = ChrY illumina rs3905 20181656..20181656 "" http://www.snpedia.com/index.php?title=Rs3905 reference = ChrY snp rs3906 20184087..20184087 "" http://www.snpedia.com/index.php?title=Rs3906 reference = ChrY affy rs3907 20069689..20069689 "" http://www.snpedia.com/index.php?title=Rs3907 reference = ChrY snp rs3908 20192556..20192556 "" http://www.snpedia.com/index.php?title=Rs3908 reference = ChrY snp rs3909 20192550..20192550 "" http://www.snpedia.com/index.php?title=Rs3909 reference = ChrY affy rs3910 20192619..20192619 "" http://www.snpedia.com/index.php?title=Rs3910 reference = ChrY snp rs3911 20192842..20192842 "" http://www.snpedia.com/index.php?title=Rs3911 reference = ChrY snp rs3912 20191727..20191727 "" http://www.snpedia.com/index.php?title=Rs3912 reference = ChrNone illumina rs3913 13299557..13299557 "" http://www.snpedia.com/index.php?title=Rs3913 reference = Chr20 snp rs3918242 44069383..44069383 "rs3918242 is one of two SNPs in the MMP9 gene associated with increased risk for myocardial infarcti..." http://www.snpedia.com/index.php?title=Rs3918242 reference = Chr20 snp rs3918396 3599765..3599765 "" http://www.snpedia.com/index.php?title=Rs3918396 reference = Chr1 both rs3922812 176926556..176926556 "Associated with type-2 diabetes in a Mexican-American population." http://www.snpedia.com/index.php?title=Rs3922812 reference = Chr6 illumina rs3923809 38548948..38548948 "This SNP, located in an intron of the BTBD9 gene, has a variant that is seen somewhat more frequentl..." http://www.snpedia.com/index.php?title=Rs3923809 reference = Chr11 affy rs3923890 124245620..124245620 "rs3923890 has been reported to be a SNP potentially associated with increased risk for autism" http://www.snpedia.com/index.php?title=Rs3923890 reference = Chr8 illumina rs3924999 32572900..32572900 "a significant association between rs3924999 and Alzheimer's disease with psychosis" http://www.snpedia.com/index.php?title=Rs3924999 reference = Chr7 illumina rs39317 116753540..116753540 "SNP rs39317 has been associated with both cholesterol levels and low-density lipoprotein levels in t..." http://www.snpedia.com/index.php?title=Rs39317 reference = Chr15 illumina rs3935591 26047607..26047607 "rs3935591 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs3935591 reference = Chr15 snp rs3940272 26142318..26142318 "rs3940272 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs3940272 reference = Chr2 both rs3948464 230758959..230758959 "associated with genetic susceptibility to tuberculosis in West Africa" http://www.snpedia.com/index.php?title=Rs3948464 reference = Chr22 snp rs3970559 17285899..17285899 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs3970559 reference = Chr2 both rs4027132 11954943..11954943 "rs4027132 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs4027132 reference = ChrNone snp rs403016 159785046..159785046 "SNP rs403016 has been reported from a study of 119 Chinese lupus patients to be associated with an i..." http://www.snpedia.com/index.php?title=Rs403016 reference = Chr16 snp rs40433 2104809..2104809 "" http://www.snpedia.com/index.php?title=Rs40433 reference = Chr19 illumina rs405509 50100676..50100676 "obstructive sleep apnea rs405509" http://www.snpedia.com/index.php?title=Rs405509 reference = ChrY affy rs4116820 20531485..20531485 "" http://www.snpedia.com/index.php?title=Rs4116820 reference = ChrY affy rs4116821 20531728..20531728 "" http://www.snpedia.com/index.php?title=Rs4116821 reference = ChrNone affy rs4129148 910180..910180 "rs4129148, located near the CSF2RA gene, has been reported in a whole genome association study to be..." http://www.snpedia.com/index.php?title=Rs4129148 reference = Chr10 snp rs41295061 6154666..6154666 "rs41295061 increases susceptibility to Type I Diabetes 1.67 times for heterozygotes (AC) and 2.27 ti..." http://www.snpedia.com/index.php?title=Rs41295061 reference = Chr5 snp rs41297577 156419081..156419081 "A study of 78 adult Thai patients infected with P. falciparum malaria reported that the TIM1 promote..." http://www.snpedia.com/index.php?title=Rs41297577 reference = Chr5 snp rs41297579 156418986..156418986 "A study of 78 adult Thai patients infected with P. falciparum malaria reported that the TIM1 promote..." http://www.snpedia.com/index.php?title=Rs41297579 reference = Chr7 snp rs41298401 128365543..128365543 "Japanese 277 SLE patients and 201 controls. Carriers of the rs2004640T slightly increased among SLE ..." http://www.snpedia.com/index.php?title=Rs41298401 reference = Chr3 illumina rs4135247 12371588..12371588 "Associated with risk of lung cancer in a Chinese population" http://www.snpedia.com/index.php?title=Rs4135247 reference = ChrNone snp rs41360247 43927160..43927160 "rs41360247 increases susceptibility to Gallstone disease 2.30 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs41360247 reference = Chr1 illumina rs4140564 184991626..184991626 "rs4140564, a SNP on chromosome 1 near the PTGS2 and PLA2G4A genes, has been associated with knee ost..." http://www.snpedia.com/index.php?title=Rs4140564 reference = ChrY illumina rs4141564 8745083..8745083 "" http://www.snpedia.com/index.php?title=Rs4141564 reference = ChrNone both rs4141886 12707867..12707867 "" http://www.snpedia.com/index.php?title=Rs4141886 reference = Chr8 illumina rs414352 55704066..55704066 "" http://www.snpedia.com/index.php?title=Rs414352 reference = Chr10 illumina rs4146894 124145371..124145371 "rs4146894, a SNP in the PLEKHA1 gene, is associated with increased risk for age related macular dege..." http://www.snpedia.com/index.php?title=Rs4146894 reference = Chr2 both rs4148217 43952937..43952937 "" http://www.snpedia.com/index.php?title=Rs4148217 reference = Chr7 snp rs4148686 116921753..116921753 "flow-mediated dilation rs4148686 (CFTR, p = 1.13*10(-5))" http://www.snpedia.com/index.php?title=Rs4148686 reference = Chr7 illumina rs4148739 86998985..86998985 "rs4148739 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs4148739 reference = Chr7 snp rs4148740 86990039..86990039 "rs4148740 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that tra..." http://www.snpedia.com/index.php?title=Rs4148740 reference = Chr12 both rs4149056 21222816..21222816 "rs4149056 is a SNP in the SLCO1B1 gene, which encodes the 'organic anion transporting polypeptide 1B..." http://www.snpedia.com/index.php?title=Rs4149056 reference = Chr9 both rs4149313 106626574..106626574 "" http://www.snpedia.com/index.php?title=Rs4149313 reference = Chr18 illumina rs4149601 53967789..53967789 "rs4149601 has been associated with hypertension. This SNP by itself was associated with diastolic bl..." http://www.snpedia.com/index.php?title=Rs4149601 reference = Chr13 snp rs4151620 47947060..47947060 "rs4151620(C;G) and rs4151620(G;G) are associated with a reduced risk of ovarian cancer compared with..." http://www.snpedia.com/index.php?title=Rs4151620 reference = Chr2 both rs419598 113603678..113603678 "May modulate other variations. Also known as the +2018T/C SNP. In a study of 113 Japanese patients w..." http://www.snpedia.com/index.php?title=Rs419598 reference = Chr6 illumina rs419788 32036778..32036778 "rs419788, a SNP in an intron of the SKIV2L gene in the MHC class III region, has been associated wit..." http://www.snpedia.com/index.php?title=Rs419788 reference = Chr16 both rs420259 23541527..23541527 "Linked to bipolar disorder in one of the most comprehensive studies to date (2007). Risk allele with..." http://www.snpedia.com/index.php?title=Rs420259 reference = Chr1 snp rs421016 153451040..153451040 "rs421016, a SNP causing an amino acid change in the GBA gene, has been determined to be the most com..." http://www.snpedia.com/index.php?title=Rs421016 reference = Chr14 snp rs421262 87470966..87470966 "" http://www.snpedia.com/index.php?title=Rs421262 reference = Chr2 both rs423904 113603733..113603733 "rs423904 increases susceptibility to Ulcerative colitis 2.60 times for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs423904 reference = Chr5 illumina rs4242182 174088774..174088774 "" http://www.snpedia.com/index.php?title=Rs4242182 reference = Chr8 both rs4242382 128586755..128586755 "rs4242383 is one of 4 tightly linked SNPs in the 'locus 1' region of 8q24 chromosomal region, which ..." http://www.snpedia.com/index.php?title=Rs4242382 reference = Chr8 both rs4242384 128587736..128587736 "[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-g..." http://www.snpedia.com/index.php?title=Rs4242384 reference = Chr10 snp rs4244285 96531606..96531606 "rs4244285 is a SNP in the CYP2C19 gene, potentially encoding the CYP2C19*2 variant. This variant is ..." http://www.snpedia.com/index.php?title=Rs4244285 reference = Chr6 illumina rs4252125 161072230..161072230 "rs4252125 or rs60784473 are the Asp472Asn described as influencing susceptibility to invasive Asperg..." http://www.snpedia.com/index.php?title=Rs4252125 reference = ChrNone snp rs4252209 4985637..4985637 "" http://www.snpedia.com/index.php?title=Rs4252209 reference = Chr7 snp rs42524 93881175..93881175 "" http://www.snpedia.com/index.php?title=Rs42524 reference = Chr10 snp rs4253208 50348728..50348728 "[omim:COCKAYNE SYNDROME, TYPE B]" http://www.snpedia.com/index.php?title=Rs4253208 reference = Chr10 snp rs4253527 81043783..81043783 "[omim:PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs4253527 reference = Chr22 illumina rs4253623 44928770..44928770 "rs4253623(G) alleles are associated with a slightly higher risk of nonfatal myocardial infarction (o..." http://www.snpedia.com/index.php?title=Rs4253623 reference = Chr17 snp rs4261597 36232062..36232062 "" http://www.snpedia.com/index.php?title=Rs4261597 reference = Chr15 snp rs4265781 40816041..40816041 "" http://www.snpedia.com/index.php?title=Rs4265781 reference = Chr3 both rs4276227 32305690..32305690 "rs4276227 has been reported in a large study to be associated with bipolar disorder. The risk allele..." http://www.snpedia.com/index.php?title=Rs4276227 reference = Chr16 both rs4280262 11554993..11554993 "" http://www.snpedia.com/index.php?title=Rs4280262 reference = Chr12 snp rs4290270 70702502..70702502 "Only for Hispanics, individuals who have a genoset composed of rs1799913(C;C) and rs4290270(T;T) are..." http://www.snpedia.com/index.php?title=Rs4290270 reference = Chr19 snp rs429358 50103781..50103781 "This SNP, located in the fourth exon of the ApoE gene, affects the amino acid at position 130 of the..." http://www.snpedia.com/index.php?title=Rs429358 reference = Chr3 illumina rs4302331 33030725..33030725 "" http://www.snpedia.com/index.php?title=Rs4302331 reference = Chr17 snp rs4340 58919624..58919624 "rs4340 is one of four SNPs representing perhaps the best studied ACE SNP. It is actually not a singl..." http://www.snpedia.com/index.php?title=Rs4340 reference = Chr17 illumina rs4344 58920456..58920456 "This SNP in the ACE gene, also known as G12269A, is reported to influence how quickly African Americ..." http://www.snpedia.com/index.php?title=Rs4344 reference = Chr8 illumina rs4355801 119993054..119993054 "[http://www.medpagetoday.com/Endocrinology/Osteoporosis/tb/9271 news] rs4355801, was associated with..." http://www.snpedia.com/index.php?title=Rs4355801 reference = Chr17 snp rs4359 58926075..58926075 "This SNP in the ACE gene, also known as C17888T, is reported to influence how quickly African Americ..." http://www.snpedia.com/index.php?title=Rs4359 reference = Chr12 illumina rs4363657 21259989..21259989 "rs4363657 is a SNP in the SLCO1B1 gene, a gene which encodes a protein involved in the liver's uptak..." http://www.snpedia.com/index.php?title=Rs4363657 reference = Chr4 illumina rs4371677 57211653..57211653 "" http://www.snpedia.com/index.php?title=Rs4371677 reference = Chr17 illumina rs4378650 35334391..35334391 "264 African American asthma subjects and 176 healthy controls. (p = 0.028 and 0.001 for rs4378650 an..." http://www.snpedia.com/index.php?title=Rs4378650 reference = Chr19 illumina rs439401 50106291..50106291 "This appears to be the snp on the Illumina Human 550 which is closest to rs4420638" http://www.snpedia.com/index.php?title=Rs439401 reference = Chr3 both rs4399848 28679467..28679467 "SNP rs4399848 (Chr 3 at 28.679467 Mb, band 3p24.1, dbSNP build 128) is associated weakly with hypert..." http://www.snpedia.com/index.php?title=Rs4399848 reference = Chr3 both rs4402960 186994381..186994381 "rs4402960 replicated as significant for type-2 diabetes risk in 1,900 Japanese patients, with odds r..." http://www.snpedia.com/index.php?title=Rs4402960 reference = Chr19 snp rs440446 50101007..50101007 "rs440446 is a SNP in an intron of the apolipoprotein E APOE gene; it is also known as the IVS1+69 va..." http://www.snpedia.com/index.php?title=Rs440446 reference = Chr5 illumina rs4415084 44698272..44698272 "rs4415084 and rs10941679 confer risk for estrogen receptor breast cancer (ER)-positive tumors (OR = ..." http://www.snpedia.com/index.php?title=Rs4415084 reference = Chr19 both rs4420638 50114786..50114786 "The researchers found that on testing DNA samples from 1,086 well-characterized Alzheimer's disease ..." http://www.snpedia.com/index.php?title=Rs4420638 reference = Chr17 illumina rs4430796 33172153..33172153 "rs4430796 is a SNP in the TCF2 gene on chromosome 17q12, associated with increased risk for prostate..." http://www.snpedia.com/index.php?title=Rs4430796 reference = Chr4 snp rs4444903 111053559..111053559 "rs4444903 is a SNP, also known as +61, located in the promoter region of the epidermal growth factor..." http://www.snpedia.com/index.php?title=Rs4444903 reference = Chr8 illumina rs444772 55701610..55701610 "" http://www.snpedia.com/index.php?title=Rs444772 reference = Chr4 affy rs4458523 6340887..6340887 "rs4458523 is in linkage disequilibrium with a polymorphism that increases susceptibility to Type II ..." http://www.snpedia.com/index.php?title=Rs4458523 reference = Chr6 illumina rs4458717 132950572..132950572 "Suspected of reproducibility problems based on [http://www.kk.org/quantifiedself/2008/05/testing-gen..." http://www.snpedia.com/index.php?title=Rs4458717 reference = Chr8 illumina rs446227 55704003..55704003 "" http://www.snpedia.com/index.php?title=Rs446227 reference = Chr18 illumina rs4464148 44713030..44713030 "rs4464148 is one of 3 SNPs in the SMAD7 gene associated with risk for colorectal cancer, based on a ..." http://www.snpedia.com/index.php?title=Rs4464148 reference = Chr20 snp rs44707 3599226..3599226 "rs44707, a SNP in the ADAM33 gene, has been linked to a predisposition to asthma and bronchial hyper..." http://www.snpedia.com/index.php?title=Rs44707 reference = ChrY affy rs4481791 19869094..19869094 "" http://www.snpedia.com/index.php?title=Rs4481791 reference = Chr15 affy rs4489954 65859129..65859129 "rs4489954, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of rest..." http://www.snpedia.com/index.php?title=Rs4489954 reference = Chr22 illumina rs450046 17281004..17281004 "[omim:HYPERPROLINEMIA, TYPE I]" http://www.snpedia.com/index.php?title=Rs450046 reference = Chr6 illumina rs4504469 24696863..24696863 "Rs4504469, a nonsynonymous SNP in exon 4 of the KIAA0319 gene, is in a region that crops up in sever..." http://www.snpedia.com/index.php?title=Rs4504469 reference = Chr10 affy rs4506565 114746031..114746031 "rs4506565 has been reported in a large study to be associated with type-2 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs4506565 reference = Chr5 both rs4532 174802756..174802756 "Implicated as part of a haplotype of the dopamine D1 receptor DRD1 gene associated with autism spect..." http://www.snpedia.com/index.php?title=Rs4532 reference = Chr8 snp rs4539 143993541..143993541 "[omim:REMOVED FROM DATABASE]" http://www.snpedia.com/index.php?title=Rs4539 reference = Chr12 snp rs45438698 5025307..5025307 "This SNP, also known as R578K, affecting an amino acid in exon 1 of the KCNA5 potassium channel gene..." http://www.snpedia.com/index.php?title=Rs45438698 reference = Chr12 snp rs45477792 5025169..5025169 "This SNP, also known as P532L, affecting an amino acid in exon 1 of the KCNA5 potassium channel gene..." http://www.snpedia.com/index.php?title=Rs45477792 reference = Chr11 affy rs4548577 46955088..46955088 "rs4548577 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteopor..." http://www.snpedia.com/index.php?title=Rs4548577 reference = Chr5 illumina rs454886 112174016..112174016 "798 invasive breast cancer cases and 843 unaffected controls *rs454886 per allele odds ratio, 1.23; ..." http://www.snpedia.com/index.php?title=Rs454886 reference = ChrMT snp rs45517935 4337..4337 "is a mitochondrial" http://www.snpedia.com/index.php?title=Rs45517935 reference = Chr2 snp rs4553808 204439250..204439250 "rs4553808, also known as A/G-1661, is a SNP in the upstream activator sequence of the cytotoxic T ly..." http://www.snpedia.com/index.php?title=Rs4553808 reference = Chr1 snp rs45539432 20848189..20848189 "rs45539432, also known as Gln456Ter or Q456X, is a SNP in the PINK1 gene. In one German family studi..." http://www.snpedia.com/index.php?title=Rs45539432 reference = Chr12 affy rs4565946 70623036..70623036 "rs4570625 and rs4565946 linked to the pathogenesis of early-onset obsessive compulsive disorder" http://www.snpedia.com/index.php?title=Rs4565946 reference = Chr1 both rs4568789 182581034..182581034 "rs4568789 (chromosome 1q25) and tagSNP rs13225697 (chromosome 7p21) to be significantly associated w..." http://www.snpedia.com/index.php?title=Rs4568789 reference = Chr12 both rs4570625 70618190..70618190 "rs4570625 and rs4565946 linked to the pathogenesis of early-onset obsessive compulsive disorder rs45..." http://www.snpedia.com/index.php?title=Rs4570625 reference = Chr6 illumina rs4576240 24704457..24704457 "" http://www.snpedia.com/index.php?title=Rs4576240 reference = ChrNone affy rs4589047 14751710..14751710 "" http://www.snpedia.com/index.php?title=Rs4589047 reference = Chr5 affy rs459552 112204655..112204655 "" http://www.snpedia.com/index.php?title=Rs459552 reference = Chr1 snp rs4606 191047795..191047795 "SNPs in the RGS2 gene, including rs4606, show association with childhood temperament, adult personal..." http://www.snpedia.com/index.php?title=Rs4606 reference = Chr11 illumina rs4606490 124247941..124247941 "rs4606490 has been reported to be a SNP potentially associated with increased risk for autism" http://www.snpedia.com/index.php?title=Rs4606490 reference = Chr1 snp rs460897 194982942..194982942 "[omim:HEMOLYTIC UREMIC SYNDROME, ATYPICAL]" http://www.snpedia.com/index.php?title=Rs460897 reference = Chr5 illumina rs4613763 40428485..40428485 "rs4613763 increases susceptibility to Crohn's disease 1.56 times for carriers of the C allele" http://www.snpedia.com/index.php?title=Rs4613763 reference = Chr16 snp rs4614723 49728676..49728676 "" http://www.snpedia.com/index.php?title=Rs4614723 reference = Chr9 affy rs4626664 9251737..9251737 "rs4626664, a SNP in the motor neuron PTPRD gene, has been linked to restless legs syndrome based on ..." http://www.snpedia.com/index.php?title=Rs4626664 reference = Chr1 snp rs4630153 63593573..63593573 "[omim:CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic]" http://www.snpedia.com/index.php?title=Rs4630153 reference = Chr22 both rs4633 18330235..18330235 "rs4633 is a variant at codon 62 of the COMT gene, however, it does not change the amino acid sequenc..." http://www.snpedia.com/index.php?title=Rs4633 reference = ChrNone snp rs4639334 32710192..32710192 "Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature] Graves' disease or m..." http://www.snpedia.com/index.php?title=Rs4639334 reference = Chr17 snp rs4646994 58919632..58919632 "rs4646994 is one of four SNPs representing perhaps the best studied ACE SNP. It is actually not a si..." http://www.snpedia.com/index.php?title=Rs4646994 reference = Chr4 snp rs4647924 1773369..1773369 "[omim:MUENKE SYNDROME]" http://www.snpedia.com/index.php?title=Rs4647924 reference = Chr11 illumina rs4648317 112836742..112836742 "rs4648317, a SNP in the dopamine D2 receptor DRD2 gene, has been linked to higher rates of smoking a..." http://www.snpedia.com/index.php?title=Rs4648317 reference = Chr1 affy rs4655595 66331347..66331347 "rs4655595 has been reported in a large study to be associated with type-2 diabetes. The risk allele ..." http://www.snpedia.com/index.php?title=Rs4655595 reference = Chr1 illumina rs4660646 42802375..42802375 "Suspected of reproducibility problems based on [http://www.kk.org/quantifiedself/2008/05/testing-gen..." http://www.snpedia.com/index.php?title=Rs4660646 reference = Chr16 illumina rs4673 87240737..87240737 "[omim:CYBA POLYMORPHISM 242C-T]" http://www.snpedia.com/index.php?title=Rs4673 reference = Chr2 snp rs4675690 208216052..208216052 "[http://originsgenomeresources.net/musings/?p=152 blog] individuals with the TT genotype at rs467569..." http://www.snpedia.com/index.php?title=Rs4675690 reference = Chr22 both rs4680 18331271..18331271 "rs4680 is a well studied SNP in the catechol-O-methyltransferase COMT gene. rs4680 is also known as ..." http://www.snpedia.com/index.php?title=Rs4680 reference = Chr3 illumina rs4684847 12361337..12361337 "Associated with at least one 'mortality outcome' in a study of ~10,000 individuals. Based on the sam..." http://www.snpedia.com/index.php?title=Rs4684847 reference = Chr4 both rs4689278 5741803..5741803 "" http://www.snpedia.com/index.php?title=Rs4689278 reference = Chr4 snp rs4696480 154826576..154826576 "preterm birth rs4696480 (T-16934A and Arg753Gln) and rs5743708) (Thr399Ile) earlier birth for infant..." http://www.snpedia.com/index.php?title=Rs4696480 reference = Chr4 snp rs4696688 7990815..7990815 "" http://www.snpedia.com/index.php?title=Rs4696688 reference = Chr5 affy rs4704397 76554198..76554198 "A study of over 9,000+ individuals indicates that each copy of rs4704397(A) is associated with an in..." http://www.snpedia.com/index.php?title=Rs4704397 reference = Chr6 illumina rs4712523 20765543..20765543 "associated with type-2 diabetes" http://www.snpedia.com/index.php?title=Rs4712523 reference = Chr6 both rs4712653 22233943..22233943 "SNPs clustered in one region of chromosome 6p22 have been linked to increased risk for the exceeding..." http://www.snpedia.com/index.php?title=Rs4712653 reference = Chr6 illumina rs4713902 35722004..35722004 "rs4713902, a SNP in the FKBP5 gene, is associated with increased risk for bipolar disorder in a stud..." http://www.snpedia.com/index.php?title=Rs4713902 reference = Chr6 both rs4714156 38469090..38469090 "rs4714156, a SNP located in the BTBD9 gene region, has been linked to a lower frequency of restless ..." http://www.snpedia.com/index.php?title=Rs4714156 reference = Chr6 illumina rs4715630 56525241..56525241 "" http://www.snpedia.com/index.php?title=Rs4715630 reference = Chr11 both rs472112 74699149..74699149 "rs472112 increases susceptibility to Substance dependence, Nicotine for carriers of the A allele [PM..." http://www.snpedia.com/index.php?title=Rs472112 reference = Chr7 both rs4728142 128361203..128361203 "rs4728142, rs3807306 and a 5 bp insertion-deletion linked multiple sclerosis in three populations" http://www.snpedia.com/index.php?title=Rs4728142 reference = Chr9 illumina rs4740283 133438117..133438117 "Implicated in type-2 diabetes based on a study of 1,161 Finnish patients." http://www.snpedia.com/index.php?title=Rs4740283 reference = Chr9 illumina rs4743056 98861432..98861432 "rs4743056 increases susceptibility to Myasthenia gravis 1.37 times for carriers of the G allele rs4..." http://www.snpedia.com/index.php?title=Rs4743056 reference = Chr11 affy rs4752946 46853484..46853484 "rs4752946 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteopor..." http://www.snpedia.com/index.php?title=Rs4752946 reference = Chr1 illumina rs4762 228912600..228912600 "rs4762, a SNP in the angiotensin II AGT gene, has been reported to be associated with increased risk..." http://www.snpedia.com/index.php?title=Rs4762 reference = Chr12 both rs4763655 9646845..9646845 "rs4763655 has been reported in a large study to be associated with multiple sclerosis. The risk alle..." http://www.snpedia.com/index.php?title=Rs4763655 reference = Chr13 affy rs4769874 30224441..30224441 "rs4769874, also known as SG13S89, is an ALOX5AP gene SNP that has been defined as part of a haplotyp..." http://www.snpedia.com/index.php?title=Rs4769874 reference = Chr15 snp rs4775765 46594929..46594929 "" http://www.snpedia.com/index.php?title=Rs4775765 reference = Chr15 illumina rs4778241 26012308..26012308 "rs4778241 is part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, f..." http://www.snpedia.com/index.php?title=Rs4778241 reference = Chr15 both rs4779584 30782048..30782048 "A study of 7000+ UK patients with colorectal cancer identified two SNPs that increase disease risk, ..." http://www.snpedia.com/index.php?title=Rs4779584 reference = Chr17 both rs4791171 60971959..60971959 "798 invasive breast cancer cases and 843 unaffected controls. rs4791171 associated with risk in prem..." http://www.snpedia.com/index.php?title=Rs4791171 reference = Chr17 both rs4792311 12855734..12855734 "[omim:PROSTATE CANCER, SUSCEPTIBILITY TO]" http://www.snpedia.com/index.php?title=Rs4792311 reference = Chr17 snp rs4792887 41232791..41232791 "family trios with suicide attempter offspring (n = 542) rs4792887 linked to suicide attempters expos..." http://www.snpedia.com/index.php?title=Rs4792887 reference = Chr17 illumina rs4794067 43163827..43163827 "rs4794067(C;C) and rs4794067(C;T) genotypes for the TBX21 gene are calculated to be at 2.15 fold hig..." http://www.snpedia.com/index.php?title=Rs4794067 reference = Chr17 snp rs4796042 30502298..30502298 "" http://www.snpedia.com/index.php?title=Rs4796042 reference = Chr17 illumina rs4796697 36912720..36912720 "" http://www.snpedia.com/index.php?title=Rs4796697 reference = Chr17 affy rs4796793 37795736..37795736 "rs4796793, a SNP in the 5' region of the signal transducer and activator 3 STAT3 gene, has been link..." http://www.snpedia.com/index.php?title=Rs4796793 reference = Chr18 both rs4799570 27240331..27240331 "" http://www.snpedia.com/index.php?title=Rs4799570 reference = Chr19 snp rs4804803 7718733..7718733 "In a study of several African populations, the (G) allele of rs4804803, a SNP in the CD209 gene, was..." http://www.snpedia.com/index.php?title=Rs4804803 reference = Chr19 illumina rs4807015 5182135..5182135 "rs1143699, rs4807015, and rs1978237 confer an increased risk of developing type-2 diabetes" http://www.snpedia.com/index.php?title=Rs4807015 reference = Chr22 snp rs4818 18331207..18331207 "Seems to play a role in the brain This is a synonymous change. it does not affect the amino acid." http://www.snpedia.com/index.php?title=Rs4818 reference = Chr11 affy rs481843 116031077..116031077 "rs481843 increases susceptibility to Elevated triglycerides for carriers of the T allele" http://www.snpedia.com/index.php?title=Rs481843 reference = Chr22 illumina rs4819756 17292678..17292678 "" http://www.snpedia.com/index.php?title=Rs4819756 reference = Chr22 both rs4821544 35588449..35588449 "A study of 507 CD patients, 475 UC patients and 576 controls from New Zealand Caucasians found that ..." http://www.snpedia.com/index.php?title=Rs4821544 reference = ChrX both rs4825476 122269160..122269160 "This SNP, located in an intron of the GRIA3 gene (also known as AMPA3), has been linked in one study..." http://www.snpedia.com/index.php?title=Rs4825476 reference = Chr6 affy rs483223 117727056..117727056 "rs483223 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocardia..." http://www.snpedia.com/index.php?title=Rs483223 reference = Chr10 affy rs4838544 50526658..50526658 "" http://www.snpedia.com/index.php?title=Rs4838544 reference = Chr1 both rs4846048 11768839..11768839 "Associated with lean body mass but not fat body mass in a study of ~1,800 Caucasians" http://www.snpedia.com/index.php?title=Rs4846048 reference = Chr3 illumina rs4855271 166197226..166197226 "" http://www.snpedia.com/index.php?title=Rs4855271 reference = Chr4 both rs4864548 56108560..56108560 "A study of 391 overweight patients concluded that the haplotype of rs1554483(G) and rs4864548(A) was..." http://www.snpedia.com/index.php?title=Rs4864548 reference = Chr1 illumina rs486907 180821180..180821180 "rs486907 is a SNP in the RNase L RNASEL gene that has been associated with cancer risk. The basic ra..." http://www.snpedia.com/index.php?title=Rs486907 reference = Chr6 affy rs4869742 151949441..151949441 "rs4869742 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone min..." http://www.snpedia.com/index.php?title=Rs4869742 reference = Chr6 illumina rs4870044 151943102..151943102 "rs4870044 increases susceptibility to Bone mineral density variations, lower for carriers of the T a..." http://www.snpedia.com/index.php?title=Rs4870044 reference = Chr9 affy rs4877365 89345512..89345512 "rs4877365 has been linked to Alzheimer's disease" http://www.snpedia.com/index.php?title=Rs4877365 reference = Chr9 illumina rs4878104 89382811..89382811 "linked to Alzheimer's disease" http://www.snpedia.com/index.php?title=Rs4878104 reference = Chr6 illumina rs4880 160033862..160033862 "The rs4880(T) allele, part of the codon for amino acid valine at codon 16 of the antioxidant protein..." http://www.snpedia.com/index.php?title=Rs4880 reference = Chr15 both rs4886605 72813041..72813041 "577 testicular germ cell tumors cases (254 seminoma, 323 nonseminoma) and 707 controls. inversely as..." http://www.snpedia.com/index.php?title=Rs4886605 reference = Chr15 snp rs4887067 76674002..76674002 "[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000125 plos] Risk Factors ..." http://www.snpedia.com/index.php?title=Rs4887067 reference = Chr22 snp rs4894 38247461..38247461 "This SNP is on its own, as well as part of a specific haplotype, associated with an overall higher r..." http://www.snpedia.com/index.php?title=Rs4894 reference = Chr6 snp rs4897081 149478231..149478231 "rs12197043 and rs4897081 novel associations in type-2 diabetes patients with nephropathy from an Afr..." http://www.snpedia.com/index.php?title=Rs4897081 reference = Chr6 snp rs4897475 131274643..131274643 "risk of cardiovascular disease rs4897475 in erythrocyte membrane protein band 4.1-like 2 (EPB41L2) a..." http://www.snpedia.com/index.php?title=Rs4897475 reference = Chr1 snp rs4908449 7215287..7215287 "affects episodic memory performance." http://www.snpedia.com/index.php?title=Rs4908449 reference = Chr20 illumina rs4911414 32193105..32193105 "rs4911414 is a SNP near the ASIP (agouti signaling protein) gene on chromosome 20. This SNP is one o..." http://www.snpedia.com/index.php?title=Rs4911414 reference = Chr3 illumina rs4917 187820407..187820407 "rs4917 is thought to regulate body fat levels and insulin sensitivity. see obesity [http://www.apoll..." http://www.snpedia.com/index.php?title=Rs4917 reference = Chr3 illumina rs4918 187821076..187821076 "Category:is a snp [http://cat.inist.fr/?aModele=afficheN&cpsidt=16815755] Homozygosity for the rs259..." http://www.snpedia.com/index.php?title=Rs4918 reference = Chr10 affy rs4919510 102724768..102724768 "discussed in [http://precedings.nature.com/documents/2127/version/1 nature]" http://www.snpedia.com/index.php?title=Rs4919510 reference = Chr14 illumina rs4934 94150556..94150556 "rs4934 increases susceptibility to Alzheimer's disease 2.56 times for (A;A) homozygotes" http://www.snpedia.com/index.php?title=Rs4934 reference = Chr10 illumina rs4935502 55625450..55625450 "" http://www.snpedia.com/index.php?title=Rs4935502 reference = Chr11 affy rs4938445 117250213..117250213 "associated with schizophrenia rs10790212-rs4938445-rs497768" http://www.snpedia.com/index.php?title=Rs4938445 reference = Chr18 illumina rs4939827 44707461..44707461 "rs4939827 is one of 3 SNPs in the SMAD7 gene associated with risk for colorectal cancer, based on a ..." http://www.snpedia.com/index.php?title=Rs4939827 reference = Chr10 illumina rs4948418 61855500..61855500 "[http://spittoon.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-..." http://www.snpedia.com/index.php?title=Rs4948418 reference = Chr1 snp rs4950928 201422505..201422505 "rs4950928 in CHI3L1 is likely to play roles in the predisposition to schizophrenia." http://www.snpedia.com/index.php?title=Rs4950928 reference = Chr2 both rs4954449 136292004..136292004 "" http://www.snpedia.com/index.php?title=Rs4954449 reference = Chr4 illumina rs4956145 109150488..109150488 "" http://www.snpedia.com/index.php?title=Rs4956145 reference = Chr5 affy rs4958803 154774673..154774673 "This SNP was identified as a 'core' SNP helping to define one (of nine total) runs of homozygosity (..." http://www.snpedia.com/index.php?title=Rs4958803 reference = Chr5 both rs4958847 150219780..150219780 "A study of 507 CD patients, 475 UC patients and 576 controls from New Zealand Caucasians found that ..." http://www.snpedia.com/index.php?title=Rs4958847 reference = Chr4 illumina rs4961 2876505..2876505 "rs4961 is a variation in the adducin 1 ADD1 gene, encoding a change from a glycine to a tryptophan, ..." http://www.snpedia.com/index.php?title=Rs4961 reference = Chr8 illumina rs4961206 87735367..87735367 "" http://www.snpedia.com/index.php?title=Rs4961206 reference = Chr4 snp rs4963 2886560..2886560 "rs4963 is in very tight linkage with rs4961, another ADD1 gene SNP, and thus linked to hypertension...." http://www.snpedia.com/index.php?title=Rs4963 reference = Chr17 both rs4968451 57282089..57282089 "rs4968451, which is in a breast cancer susceptibility gene, was associated with increased risk of me..." http://www.snpedia.com/index.php?title=Rs4968451 reference = Chr1 both rs4970834 109616403..109616403 "rs599839 and rs4970834 explain about 1% of the variation in circulating LDL-cholesterol levels. 'Whe..." http://www.snpedia.com/index.php?title=Rs4970834 reference = Chr2 illumina rs4972946 230857352..230857352 "" http://www.snpedia.com/index.php?title=Rs4972946 reference = Chr9 both rs4977574 22088574..22088574 "rs4977574 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AG) and ..." http://www.snpedia.com/index.php?title=Rs4977574 reference = Chr11 snp rs497768 117255950..117255950 "Category:is a snp associated with schizophrenia rs10790212-rs4938445-rs497768" http://www.snpedia.com/index.php?title=Rs497768 reference = Chr9 illumina rs4978584 116226533..116226533 "" http://www.snpedia.com/index.php?title=Rs4978584 reference = ChrNone snp rs498055 97344904..97344904 "rs498055 was initially suspected of being a factor in Alzheimer's disease, but later work could not..." http://www.snpedia.com/index.php?title=Rs498055 reference = Chr11 illumina rs4986761 107629971..107629971 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs4986761 reference = Chr17 illumina rs4986764 57118129..57118129 "" http://www.snpedia.com/index.php?title=Rs4986764 reference = Chr9 illumina rs4986790 119515123..119515123 "rs4986790, a SNP also known as Asp299Gly in the TLR4 gene, is often studied along with a cosegregati..." http://www.snpedia.com/index.php?title=Rs4986790 reference = Chr9 illumina rs4986791 119515423..119515423 "rs4986791, a SNP also known as Thr399Ile in the TLR4 gene, is often studied along with a cosegregati..." http://www.snpedia.com/index.php?title=Rs4986791 reference = Chr17 illumina rs4986850 38498997..38498997 "This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs4986850 reference = Chr17 illumina rs4986852 38497955..38497955 "[omim:BREAST-OVARIAN CANCER]" http://www.snpedia.com/index.php?title=Rs4986852 reference = Chr10 snp rs4986893 96530400..96530400 "rs4986893 is a SNP in the CYP2C19 gene, potentially encoding the CYP2C19*3 variant. This variant has..." http://www.snpedia.com/index.php?title=Rs4986893 reference = Chr13 affy rs4987047 31851529..31851529 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs4987047 reference = Chr8 snp rs4987076 18124281..18124281 "[omim:NAT1*17 ALLELE]" http://www.snpedia.com/index.php?title=Rs4987076 reference = Chr13 illumina rs4987117 31812236..31812236 "This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, bu..." http://www.snpedia.com/index.php?title=Rs4987117 reference = Chr2 illumina rs4987188 47496961..47496961 "[omim:MSH2 POLYMORPHISM]" http://www.snpedia.com/index.php?title=Rs4987188 reference = Chr11 affy rs4987945 107627802..107627802 "This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but ..." http://www.snpedia.com/index.php?title=Rs4987945 reference = Chr2 illumina rs4988235 136325116..136325116 "Also known as 'C/T(-13910)', and located in the MCM6 gene but with influence on the lactase LCT gene..." http://www.snpedia.com/index.php?title=Rs4988235 reference = Chr11 both rs4988300 67845407..67845407 "linked to obesity" http://www.snpedia.com/index.php?title=Rs4988300 reference = Chr11 snp rs4988321 67930765..67930765 "rs4988321 is a SNP in the LRP5 gene that is also known as Val667Met; the more common (G) allele enco..." http://www.snpedia.com/index.php?title=Rs4988321 reference = ChrY illumina rs4988808 7278079..7278079 "" http://www.snpedia.com/index.php?title=Rs4988808 reference = Chr6 snp rs4988889 32742930..32742930 "Source [http://www.nature.com/ng/journal/v38/n10/fig_tab/ng1885_T1.html nature] Celiac diseased rs49..." http://www.snpedia.com/index.php?title=Rs4988889 reference = Chr8 illumina rs4994 37942955..37942955 "rs4994, also known as the Arg64 variant, is a SNP in the ADRB3 gene. The rs4994(C) allele encodes th..." http://www.snpedia.com/index.php?title=Rs4994 reference = Chr10 affy rs501120 44073873..44073873 "rs501120 is a SNP found to be associated with heart disease in two populations by the German MI (Myo..." http://www.snpedia.com/index.php?title=Rs501120 reference = Chr10 both rs5015480 94455539..94455539 "associated with type-2 diabetes" http://www.snpedia.com/index.php?title=Rs5015480 reference = Chr19 snp rs5020278 9186116..9186116 "rs5020278, a SNP in the OR7DR olfactory receptor gene, is associated with how individuals perceive t..." http://www.snpedia.com/index.php?title=Rs5020278 reference = Chr6 affy rs5029939 138237416..138237416 "An association was found between Systemic lupus erythematosus (SLE) and rs5029939 (meta-analysis p =..." http://www.snpedia.com/index.php?title=Rs5029939 reference = Chr19 snp rs5030341 10244275..10244275 "[http://genetics.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.pgen.0030120...." http://www.snpedia.com/index.php?title=Rs5030341 reference = Chr22 snp rs5030655 40855030..40855030 "The (-) form of this SNP, representing a deletion of one nucleotide, causes a frameshift such that t..." http://www.snpedia.com/index.php?title=Rs5030655 reference = Chr12 snp rs5030849 101770783..101770783 "[omim:PHENYLKETONURIA, MILD]" http://www.snpedia.com/index.php?title=Rs5030849 reference = Chr10 illumina rs5030882 70122477..70122477 "Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio..." http://www.snpedia.com/index.php?title=Rs5030882 reference = Chr17 illumina rs5036 39694471..39694471 "[omim:BAND 3 MEMPHIS]" http://www.snpedia.com/index.php?title=Rs5036 reference = Chr1 illumina rs5051 228916495..228916495 "rs5051 is a SNP in the promoter of the angiotensin AGT gene, and presumably due to it's tight linkag..." http://www.snpedia.com/index.php?title=Rs5051 reference = Chr1 both rs505151 55301775..55301775 "rs505151 rs562556 show evidence of 'gain-of-function' mutations that are associated with higher LDL ..." http://www.snpedia.com/index.php?title=Rs505151 reference = Chr1 both rs5065 11828655..11828655 "rs5065, also known as T2238C, is a SNP in the atrial natriuretic precursor A NPPA gene. A large stud..." http://www.snpedia.com/index.php?title=Rs5065 reference = Chr1 illumina rs5067 11828568..11828568 "rs5067 is a SNP in the natriuretic peptide precursor A NPPA gene. In a study of ~500 asthma patients..." http://www.snpedia.com/index.php?title=Rs5067 reference = Chr1 illumina rs5082 159460307..159460307 "rs5082 is a SNP in the apolipoprotein APOA2 gene, and may influence obesity and heart disease risk. ..." http://www.snpedia.com/index.php?title=Rs5082 reference = Chr1 both rs509749 159060184..159060184 "rs509749 is a SNP in exon 8 of the LY9 gene; this SNP is also known as Met602Val. The (A) allele enc..." http://www.snpedia.com/index.php?title=Rs509749 reference = Chr20 illumina rs512625 3596378..3596378 "rs512625 was associated with psoriasis in a study of 150 French adults." http://www.snpedia.com/index.php?title=Rs512625 reference = Chr1 illumina rs5174 53485315..53485315 "rs5174 encodes a variant of the LRP8 gene, encoding the low density lipoprotein receptor-related 8 p..." http://www.snpedia.com/index.php?title=Rs5174 reference = Chr3 snp rs5186 149942678..149942678 "rs5186 is a SNP known as +1166A/C, located in the 3' untranslated region of the angiotensin II recep..." http://www.snpedia.com/index.php?title=Rs5186 reference = Chr2 both rs520354 21113117..21113117 "rs520354 is a SNP in an intron of the apolipoprotein B APOB gene; it is also known as the IVS6+360C>..." http://www.snpedia.com/index.php?title=Rs520354 reference = Chr11 illumina rs521102 125019783..125019783 "rs521102, also known as IVS11 +35, G>A, is a SNP in the CHEK1 gene. In a study of 119 American patie..." http://www.snpedia.com/index.php?title=Rs521102 reference = Chr11 both rs5215 17365206..17365206 "The association between type-1 diabetes and rs5215 is mentioned as being replicated in ; there is al..." http://www.snpedia.com/index.php?title=Rs5215 reference = Chr11 snp rs5219 17366148..17366148 "The association between type-1 diabetes and rs5219 is mentioned as being replicated in ; there is al..." http://www.snpedia.com/index.php?title=Rs5219 reference = Chr2 snp rs523349 31659210..31659210 "rs523349 is a SNP in the steroid-5-alpha-reductase SRD5A2 gene; it is also known as V89L. In a study..." http://www.snpedia.com/index.php?title=Rs523349 reference = Chr10 snp rs523747 13206082..13206082 "" http://www.snpedia.com/index.php?title=Rs523747 reference = Chr1 snp rs5253 16252783..16252783 "" http://www.snpedia.com/index.php?title=Rs5253 reference = Chr19 snp rs527221 50967816..50967816 "" http://www.snpedia.com/index.php?title=Rs527221 reference = Chr1 illumina rs5275 184909681..184909681 "rs5275, also known as exon1-+837T>C, is a SNP in the PRGS2 gene. A study of 635 Caucasian bladder ca..." http://www.snpedia.com/index.php?title=Rs5275 reference = Chr6 illumina rs529038 117728926..117728926 "" http://www.snpedia.com/index.php?title=Rs529038 reference = Chr6 illumina rs529156 117728881..117728881 "" http://www.snpedia.com/index.php?title=Rs529156 reference = Chr5 both rs532964 78376042..78376042 "" http://www.snpedia.com/index.php?title=Rs532964 reference = Chr4 both rs5333 148680487..148680487 "In 630 patients with essential hypertension (EHT) among males significant differences in rs5351 and ..." http://www.snpedia.com/index.php?title=Rs5333 reference = Chr4 snp rs5335 148683290..148683290 "rs5335, a SNP in the EDNRA gene, has been associated with a (slightly) increased risk for hypertensi..." http://www.snpedia.com/index.php?title=Rs5335 reference = Chr4 both rs534654 55984977..55984977 "Along with rs6442925 and rs1534891, this SNP, rs534654, is part of a 3-SNP (multi-locus) interaction..." http://www.snpedia.com/index.php?title=Rs534654 reference = Chr13 both rs5351 77373314..77373314 "In 630 patients with essential hypertension (EHT) among males significant differences in rs5351 and ..." http://www.snpedia.com/index.php?title=Rs5351 reference = Chr13 illumina rs5352 77373231..77373231 "[omim:HIRSCHSPRUNG DISEASE 2]" http://www.snpedia.com/index.php?title=Rs5352 reference = Chr1 illumina rs5361 167967684..167967684 "The rs5361 Ser128Arg variation in this gene, known as E-selectin, is linked to several thrombotic di..." http://www.snpedia.com/index.php?title=Rs5361 reference = Chr6 illumina rs5370 12404241..12404241 "[http://www.genome.jp/dbget-bin/www_bget?omim+131240 omim 131240] In a study of 103 candidate genes ..." http://www.snpedia.com/index.php?title=Rs5370 reference = Chr3 illumina rs5400 172214994..172214994 "rs5400(T;T) carriers had a significantly higher intake of sugars [http://skeptalchemist.blogspot.com..." http://www.snpedia.com/index.php?title=Rs5400 reference = Chr6 both rs540825 154456139..154456139 "[http://www.psychiatrictimes.com/display/article/10168/1153657 Psychiatric Times] This SNP is locate..." http://www.snpedia.com/index.php?title=Rs540825 reference = Chr12 snp rs5443 6825136..6825136 "rs5443, a SNP in the G-protein beta3 subunit (GNB3) gene that is more commonly known as the C825T va..." http://www.snpedia.com/index.php?title=Rs5443 reference = Chr6 illumina rs547154 32018917..32018917 "rs547154 significantly associated with Age-related maculopathy in both our case-control (P-value 0.0..." http://www.snpedia.com/index.php?title=Rs547154 reference = Chr19 illumina rs5498 10256683..10256683 "rs5498, also known as E469K or K469E, is a SNP in the ICAM1 gene that has been associated in some st..." http://www.snpedia.com/index.php?title=Rs5498 reference = ChrX snp rs551492 73488714..73488714 "" http://www.snpedia.com/index.php?title=Rs551492 reference = Chr4 both rs5522 149576925..149576925 "" http://www.snpedia.com/index.php?title=Rs5522 reference = Chr13 both rs557337 74759002..74759002 "" http://www.snpedia.com/index.php?title=Rs557337 reference = Chr6 snp rs55994263 160446898..160446898 "rs8191962 is also known as rs55994263 association with type-2 diabetes located within the hsa-miR-65..." http://www.snpedia.com/index.php?title=Rs55994263 reference = Chr11 both rs560096 68435538..68435538 "" http://www.snpedia.com/index.php?title=Rs560096 reference = Chr2 both rs560887 169471394..169471394 "rs560887, p = 4 x 10(-7)) *654 normoglycemic subjects, replicated in 9,353 subjects *fasting plasma ..." http://www.snpedia.com/index.php?title=Rs560887 reference = Chr13 snp rs561241 112808035..112808035 "risk of cardiovascular disease rs561241 for hemostatic factors was p = 4.5*10(-16)" http://www.snpedia.com/index.php?title=Rs561241 reference = Chr1 snp rs562556 55296825..55296825 "rs505151 rs562556 show evidence of 'gain-of-function' mutations that are associated with higher LDL ..." http://www.snpedia.com/index.php?title=Rs562556 reference = Chr9 both rs564398 22019547..22019547 "[http://suicyte.wordpress.com/20