Chromosome 9
339 well-documented SNPs on chromosome 9, in order of position (GRCh38).
- rs6476030DOCK8 · 289,061A;ANo summary available.Typical
- rs10975200KANK1 · 571,085A;ANo summary available.Typical
- rs98867841,521,204A;Amixed evidence of Alzheimer's disease riskMinor
- rs2296212SMARCA2 · 2,191,309C;Ccommon in complete genomicsTypical
- rs564816GLIS3 · 4,015,370C;Ccommon genotypeTypical
- rs104917344,482,706T;T1.4x risk of early onset OCDTypical
- rs2228622SLC1A1 · 4,564,432G;Gcommon in clinvarTypical
- rs12682807SPATA6L · 4,574,022A;Acommon in clinvarTypical
- rs301430SLC1A1 · 4,576,680T;Tcommon in clinvarTypical
- rs3087879SLC1A1 · 4,586,808G;Gcommon in clinvarTypical
- rs10974944INSL6 · 5,070,831G;G2 - 4 fold increased odds of V617F-associated MPNsImportant
- rs4495487JAK2 · 5,072,798C;C2 - 4 fold increased odds of developing V617F-associated MPNsImportant
- rs77375493JAK2 · 5,073,770G;TJAK2-V617F variant presentVery important
- rs12343867INSL6 · 5,074,189C;C2 - 4 fold increased odds of developing V617F-associated MPNsImportant
- rs12340895INSL6 · 5,076,691G;G2 - 4 fold increased odds of developing V617F-positive MPNImportant
- rs2230724INSL6 · 5,081,780G;Gcommon in clinvarTypical
- rs3780374JAK2 · 5,099,677A;ASubstantially increased odds of developing V617F-positive MPN.Worth knowing
- rs2797512ERMP1 · 5,807,444T;Tcommon in complete genomicsTypical
- rs7037276IL33 · 6,247,430T;TNo summary available.Typical
- rs7197256,365,683A;A1.46x increased risk for colorectal cancerTypical
- rs121964976GLDC · 6,589,230G;GGlycine encephalopathy; Non-ketotic hyperglycinemiaVery important
- rs16928280PTPRD · 8,695,233T;Tcommon genotypeTypical
- rs6477346PTPRD · 8,749,291C;Ccommon in complete genomicsTypical
- rs10116682PTPRD · 8,761,778C;Ccommon in complete genomicsTypical
- rs1975197PTPRD · 8,846,955A;A>1.3x increased risk of developing restless legs syndromeWorth knowing
- rs4626664PTPRD · 9,261,737A;A>1.44x increased risk of developing restless legs syndromeWorth knowing
- rs7849581PTPRD · 9,924,724C;Ccommon genotypeTypical
- rs291272PTPRD · 10,043,014T;Tcommon genotypeTypical
- rs1692909712,521,826G;Gcommon genotypeTypical
- rs140879912,672,097C;CNo summary available.Typical
- rs2733832TYRP1 · 12,704,725C;Ccommon in clinvarTypical
- rs1063380TYRP1 · 12,710,090T;Tcommon in clinvarTypical
- rs1360517LOC107987047 · 13,007,130C;THigher susceptibility for AIDSMinor
- rs13297480MPDZ · 13,219,571T;Tcommon in complete genomicsTypical
- rs1096153414,470,835A;Acommon in complete genomicsTypical
- rs1780159LOC105375981 · 15,157,979T;Tcommon on affy axiom dataTypical
- rs471364TTC39B · 15,289,580T;Tcommon in complete genomicsTypical
- rs381411316,915,023C;C0.8x decreased risk for ovarian cancerMinor
- rs1081086517,895,107T;Tcommon on affy axiom dataTypical
- rs2210327ADAMTSL1 · 18,109,237A;Acommon in complete genomicsTypical
- rs1125488IFNE · 21,481,557T;Tcommon in complete genomicsTypical
- rs7023954MTAP · 21,816,759G;Gcommon in clinvarTypical
- rs7027989MTAP · 21,817,755A;A1.26x increased myocardial infarction riskTypical
- rs3731249CDKN2A · 21,970,917C;Ccommon in clinvarTypical
- rs768966657CDKN2A · 21,971,021-;GACFor those w/ cancer, a slightly worse prognosis; also, slightly increased melanoma riskVery important
- rs587776716CDKN2A · 21,971,115-;-Significantly increased risk for melanoma and pancreatic cancerVery important
- rs3731245CDKN2A · 21,972,446C;Ccommon in complete genomicsTypical
- rs3731239CDKN2A · 21,974,219G;G0.9x lower risk for breast cancerTypical
- rs777948908CDKN2A · 21,974,722C;GMalignant melanoma predisposing mutationVery important
- rs746834149CDKN2A · 21,974,724C;TMalignant melanoma predisposing mutationVery important
- rs2811712CDKN2BAS · 21,998,036G;G>1.5x less risk for physical impairment with age.Worth knowing
- rs3218005CDKN2BAS · 22,000,248C;CSlightly higher (1.55x) risk for breast cancerMinor
- rs3217992CDKN2B · 22,003,224T;T1.24x increased myocardial infarction riskTypical
- rs1063192CDKN2B · 22,003,368G;G0.71x reduced risk of myocardial infarctionMinor
- rs3217989CDKN2B · 22,003,791T;Tcommon in complete genomicsTypical
- rs17756311CDKN2B-AS1 · 22,053,896A;APossible higher risk of childhood acute lymphoblastic leukemiaMinor
- rs1011970CDKN2B-AS1 · 22,062,135G;Gcommon in complete genomicsTypical
- rs4977756CDKN2BAS · 22,068,653G;G1.93x higher risk for glioma developmentMinor
- rs10116277CDKN2B-AS1 · 22,081,398G;TNo summary available.Typical
- rs1333040CDKN2BAS · 22,083,405C;CnormalTypical
- rs10757272CDKN2B-AS1 · 22,088,261T;T1.54x increased risk for Coronary artery diseaseWorth knowing
- rs10757274CDKN2B-AS1 · 22,096,056A;AnormalTypical
- rs4977574CDKN2B-AS1 · 22,098,575G;GMost studies find a somewhat elevated (~1.5x) risk for myocardial infarctionMinor
- rs2383206CDKN2BAS · 22,115,027G;G1.7x increased risk for heart diseaseImportant
- rs10965235CDKN2B-AS1 · 22,115,106C;Ccommon in complete genomicsTypical
- rs2383207CDKN2BAS · 22,115,960G;Gincreased risk for heart diseaseWorth knowing
- rs1075727822,124,478G;G1.6x risk for Heart Attack; 1.3x risk for Abdominal Aortic Aneurysm and Brain Aneurysm.Worth knowing
- rs133304822,125,348C;C1.5x increased coronary artery disease risk; 2x increased periodontitis riskWorth knowing
- rs133304922,125,504C;C1.9x increased risk for coronary artery diseaseVery important
- rs1081166122,134,095T;T1.2x increased risk for type-2 diabetesWorth knowing
- rs613391LOC107987054 · 22,670,716G;Gcommon in complete genomicsTypical
- rs1255273625,449,124T;Tcommon in complete genomicsTypical
- rs1330028425,452,814G;Gcommon in complete genomicsTypical
- rs17774966LOC105375996 · 25,551,359C;Ccommon on affy axiom dataTypical
- rs497805326,208,859G;Gcommon genotypeTypical
- rs1329458926,694,890A;Acommon in complete genomicsTypical
- rs7045881PLAA · 26,935,998A;Acommon on affy axiom dataTypical
- rs12003612PLAA · 26,940,725C;CNo summary available.Minor
- rs682632TEK · 27,183,465C;Ccommon in complete genomicsTypical
- rs639225TEK · 27,202,872A;Acommon in clinvarTypical
- rs80338908TEK · 27,206,762C;Ttendency for multiple cutaneous and mucosal venous malformationsVery important
- rs2814707LOC107987057 · 27,536,399T;T>1.2x increased risk for ALSMinor
- rs3849942LOC107987057 · 27,543,283T;T1.4x increased risk for ALSMinor
- rs1081337430,879,677A;Acommon genotypeTypical
- rs457650631,546,474G;Gcommon genotypeTypical
- rs17288067ACO1 · 32,409,048G;GNo summary available.Typical
- rs1097117032,870,070G;Gcommon genotypeTypical
- rs11792454APTX · 33,011,999C;CNo summary available.Typical
- rs17324630APTX · 33,013,140T;TNo summary available.Typical
- rs17324756APTX · 33,014,687T;TNo summary available.Typical
- rs10971319APTX · 33,015,016G;GNo summary available.Typical
- rs1556249APTX · 33,020,223C;CNo summary available.Typical
- rs10971346DNAJA1 · 33,031,085G;GNo summary available.Typical
- rs16918958DNAJA1 · 33,036,930C;CNo summary available.Typical
- rs12336160CHMP5 · 33,283,584G;Gcommon in complete genomicsTypical
- rs4879809SIGMAR1 · 34,635,601T;Tcommon in clinvarTypical
- rs111033640GALT · 34,646,586-;-Galactosemia (homozygous Duarte mutation)Very important
- rs111033690GALT · 34,647,858T;TGalactosemia (predicted); see discussionVery important
- rs75391579GALT · 34,648,170G;GGalactosemia (predicted); see discussionVery important
- rs2070075GALT · 34,648,421C;Ccommon in complete genomicsTypical
- rs17845454GALT · 34,649,445A;ANo summary available.Typical
- rs2070074GALT · 34,649,445G;Gharmless ancestral formMinor
- rs11575580IL11RA · 34,660,867C;Ccommon genotypeTypical
- rs951005LOC101929761 · 34,743,684A;Acommon in complete genomicsTypical
- rs13293564UNC13B · 35,166,766G;G1.63x increased nephropathy risk among type-1 diabeticsTypical
- rs4879926TLN1 · 35,700,840T;Tcommon genotypeTypical
- rs16932912RECK · 36,087,879G;Gcommon in complete genomicsTypical
- rs6476606PAX5 · 37,005,564G;Gcommon/normalTypical
- rs1329568POMT2 · 37,037,979G;Gcommon in complete genomicsTypical
- rs80356708GRHPR · 37,424,864-;-Primary HyperoxaluriaVery important
- rs2228093ALDH1B1 · 38,396,005T;TAssociated with alcohol-induced hypersensitivity reactionsImportant
- rs104894108FXN · 69,035,785A;AFriedreich's ataxiaVery important
- rs2309428TJP2 · 69,228,107A;Acommon in complete genomicsTypical
- rs2282335TJP2 · 69,251,016G;Gcommon in clinvarTypical
- rs1796993TMC1 · 72,700,522G;Gcommon in complete genomicsTypical
- rs8187974ALDH1A1 · 72,911,950A;AGreater alcohol consumptionWorth knowing
- rs375835473,149,649A;Acommon on affy axiom dataTypical
- rs1114360973,543,766G;Gcommon on affy axiom dataTypical
- rs2274924TRPM6 · 74,761,731T;Tcommon in clinvarTypical
- rs3750425TRPM6 · 74,762,494C;Ccommon in clinvarTypical
- rs11144134TRPM6 · 74,884,880T;Tcommon on affy axiom dataTypical
- rs1051204975,661,759C;Ccommon in complete genomicsTypical
- rs1234448875,811,009G;Gcommon on affy axiom dataTypical
- rs11144688PCSK5 · 75,927,370G;Gcommon on affy axiom dataTypical
- rs1329213679,337,213C;Ccommon on affy axiom dataTypical
- rs237838379,424,447A;Acommon on affy axiom dataTypical
- rs1255499979,427,576C;Ccommon genotypeTypical
- rs1086775281,400,122C;Ccommon on affy axiom dataTypical
- rs10867921RASEF · 82,994,866G;Gcommon genotypeTypical
- rs10868025FRMD3 · 83,549,261G;GNo summary available.Typical
- rs7853758LOC105376116 · 84,286,011G;Gcommon in clinvarTypical
- rs11568388LOC105376116 · 84,290,204C;Ccommon in complete genomicsTypical
- rs885004SLC28A3 · 84,294,635G;Gcommon in clinvarTypical
- rs1122530NTRK2 · 84,849,437A;Acommon in complete genomicsTypical
- rs2289658NTRK2 · 84,948,455T;Tcommon in complete genomicsTypical
- rs2289657NTRK2 · 84,948,545C;Ccommon in complete genomicsTypical
- rs2289656NTRK2 · 84,948,647G;GNo summary available.Typical
- rs7019241GOLM1 · 86,078,545C;CaverageTypical
- rs10868366GOLM1 · 86,085,145C;CNo summary available.Typical
- rs1114159786,912,543A;Acommon genotypeTypical
- rs1806864LOC100287242 · 87,416,754G;Gcommon on affy axiom dataTypical
- rs4878104DAPK1 · 87,578,076C;TNo summary available.Typical
- rs11526468SEMA4D · 89,388,764C;Ccommon in complete genomicsTypical
- rs13284404SEMA4D · 89,402,909C;Ccommon in complete genomicsTypical
- rs10993738SYK · 90,870,958A;Acommon in complete genomicsTypical
- rs29176690,905,456T;Tcommon in complete genomicsTypical
- rs119482081SPTLC1 · 92,080,045C;THereditary sensory neuropathy, type 1Very important
- rs16936752WNK2 · 93,301,408T;Tcommon in complete genomicsTypical
- rs125776394,131,663G;Gcommon genotypeTypical
- rs1099316094,306,644A;Acommon in complete genomicsTypical
- rs1691006194,552,459G;Gcommon in complete genomicsTypical
- rs1769259FBP1 · 94,606,867T;Tcommon in complete genomicsTypical
- rs10821415C9orf3 · 94,951,177C;Ccommon/normalTypical
- rs3802458C9orf3 · 94,978,992A;Acommon on affy axiom dataTypical
- rs3802457C9orf3 · 94,979,054G;Gcommon genotypeTypical
- rs357564PTCH1 · 95,447,312G;Gcommon in clinvarTypical
- rs2236405PTCH1 · 95,449,290T;Tcommon in clinvarTypical
- rs16909898LOC100507346 · 95,468,726A;Acommon in complete genomicsTypical
- rs2066836PTCH1 · 95,476,076G;Gcommon in clinvarTypical
- rs473902PTCH1 · 95,493,953T;Tcommon genotypeTypical
- rs1098880295,614,417G;Gcommon in complete genomicsTypical
- rs1179099495,666,984C;Ccommon in complete genomicsTypical
- rs2066479HSD17B3 · 96,235,528C;Ccommon in clinvarTypical
- rs9409407HSD17B3 · 96,292,967G;Gcommon in complete genomicsTypical
- rs10816533ZNF510 · 96,776,856G;Gcommon genotypeTypical
- rs6477872TCEA1P1 · 97,069,874T;Tcommon/normalTypical
- rs3176683XPA · 97,686,335A;Acommon in complete genomicsTypical
- rs1800975XPA · 97,697,296T;Tcommon in clinvarTypical
- rs1081793897,700,127T;Tcommon genotypeTypical
- rs785025897,786,731G;GSlightly higher odds of developing primary hypothyroidism.Minor
- rs96551397,793,827A;A3.1x increased thyroid cancer riskWorth knowing
- rs2184026GABBR2 · 98,542,066C;Ccommon in complete genomicsTypical
- rs3750344GABBR2 · 98,578,034T;Tcommon in complete genomicsTypical
- rs703446299,095,919C;Ccommon in complete genomicsTypical
- rs334353TGFBR1 · 99,146,083T;Tcommon in clinvarTypical
- rs334354TGFBR1 · 99,146,633A;AAssociated with cancer risk, but controversialTypical
- rs868TGFBR1 · 99,149,374A;Acommon in clinvarTypical
- rs334348TGFBR1 · 99,150,189A;Acommon in clinvarTypical
- rs334349TGFBR1 · 99,152,105G;Gcommon in clinvarTypical
- rs1590TGFBR1 · 99,153,883T;Tcommon in clinvarTypical
- rs64905799,472,041C;CNo summary available.Typical
- rs2491097INVS · 100,240,169C;Ccommon on affy axiom dataTypical
- rs1572983BAAT · 101,371,346C;Ccommon in clinvarTypical
- rs1800546ALDOB · 101,427,574C;GCarrier of a hereditary fructose intolerance (HFI) mutationImportant
- rs1407877LOC105376186 · 101,593,173C;Ccommon in complete genomicsTypical
- rs10989591GRIN3A · 101,686,816C;CcommonTypical
- rs12551885104,066,123G;Gcommon genotypeTypical
- rs363717ABCA1 · 104,782,419C;Ccommon in clinvarTypical
- rs4149339ABCA1 · 104,782,875G;Gcommon in clinvarTypical
- rs4149338ABCA1 · 104,783,622G;Gcommon in clinvarTypical
- rs2230808ABCA1 · 104,800,523T;Tcommon in clinvarTypical
- rs2297404ABCA1 · 104,802,185G;GNo summary available.Typical
- rs2066714ABCA1 · 104,824,472T;Tcommon in clinvarTypical
- rs2066715ABCA1 · 104,825,752C;Ccommon in complete genomicsTypical
- rs2853579ABCA1 · 104,828,991G;Gcommon in clinvarTypical
- rs2515629ABCA1 · 104,832,083A;Acommon in complete genomicsTypical
- rs9282541ABCA1 · 104,858,554G;GcommonTypical
- rs4149274ABCA1 · 104,877,133G;GAssociated with higher HDL (good) cholesterol.Minor
- rs4149268ABCA1 · 104,884,939C;Tassociated with higher HDL cholesterolWorth knowing
- rs3890182ABCA1 · 104,885,374A;ANo summary available.Typical
- rs3905000ABCA1 · 104,894,789G;Gcommon in complete genomicsTypical
- rs1800977LOC105376196 · 104,928,169G;Gcommon/normalTypical
- rs193008SLC44A1 · 105,280,525T;Tcommon in complete genomicsTypical
- rs34006675FKTN · 105,604,218G;Gcommon in complete genomicsTypical
- rs1463984TAL2 · 105,664,781C;Ccommon in complete genomicsTypical
- rs4742971105,892,815G;Gcommon on affy axiom dataTypical
- rs2090409106,204,807C;Cage at menarche ~2 months later on averageTypical
- rs10816625LOC105376214 · 108,074,792A;Gslightly increased risk for breast cancer (1.12x)Minor
- rs13294895LOC105376214 · 108,074,895C;Tslightly increased risk for breast cancer (1.09x)Minor
- rs1538660IKBKAP · 108,879,545A;GLikely to be a benign variantTypical
- rs3204145IKBKAP · 108,889,340A;TLikely to be a benign variantTypical
- rs111033171IKBKAP · 108,899,816G;GFamilial dysautonomiaVery important
- rs137853022IKBKAP · 108,900,303G;GFamilial dysautonomiaVery important
- rs17853166IKBKAP · 108,917,660T;TNormalTypical
- rs643410TMEM245 · 109,037,283C;Ccommon genotypeTypical
- rs523340C9orf5 · 109,091,966G;Gcommon on affy axiom dataTypical
- rs1327533SVEP1 · 110,368,883T;Tcommon in complete genomicsTypical
- rs7042161SVEP1 · 110,434,983C;Ccommon in complete genomicsTypical
- rs578430MUSK · 110,800,863G;Gcommon in complete genomicsTypical
- rs10980705LPAR1 · 111,040,905T;T3.7x increased risk for knee osteoarthritisWorth knowing
- rs2782931SUSD1 · 112,087,910T;TNo summary available.Typical
- rs16917040KIAA1958 · 112,519,756T;Tcommon in complete genomicsTypical
- rs10817408112,925,455T;TnormalTypical
- rs1800435ALAD · 113,391,611C;GCarrier of an ALAD deficiency porphyria mutationImportant
- rs7868992COL27A1 · 114,228,791A;A1.29x risk of Tourette's SyndromeTypical
- rs2274158WHRN · 114,403,926G;Gcommon in clinvarTypical
- rs2274159WHRN · 114,403,966A;Acommon in clinvarTypical
- rs6478078WHRN · 114,404,058C;Ccommon in complete genomicsTypical
- rs942519WHRN · 114,406,753A;Acommon in clinvarTypical
- rs12339210WHRN · 114,407,961G;Gcommon in clinvarTypical
- rs4978584WHRN · 114,424,432C;Ccommon in clinvarTypical
- rs10817610WHRN · 114,426,286C;Ccommon in clinvarTypical
- rs10982256WHRN · 114,498,554C;C1.5x riskTypical
- rs6478105114,754,905A;ANo summary available.Typical
- rs4979462TNFSF15 · 114,804,733T;TIncreased risk of developing primary biliary cirrhosisWorth knowing
- rs2006996114,830,358T;Tcommon in complete genomicsTypical
- rs10982724DEC1 · 115,395,450T;Tcommon in complete genomicsTypical
- rs10983755TLR4 · 117,702,392G;Gcommon in complete genomicsTypical
- rs10759932TLR4 · 117,702,866C;Cincreased risk for chorionic plate inflammationWorth knowing
- rs11536869TLR4 · 117,707,554A;Acommon genotypeTypical
- rs1927911TLR4 · 117,707,776G;GnormalTypical
- rs11536879TLR4 · 117,709,933A;ANo summary available.Typical
- rs5030729TLR4 · 117,712,061A;Acommon in complete genomicsTypical
- rs4986790TLR4 · 117,713,024G;Gcomplex; numerous associations reportedWorth knowing
- rs4986791TLR4 · 117,713,324T;Tcomplex; see detailsWorth knowing
- rs5030719TLR4 · 117,713,658G;Gcommon in complete genomicsTypical
- rs11536897TLR4 · 117,717,732G;Gcommon in complete genomicsTypical
- rs1554973TLR4 · 117,718,534C;Cincreased risk for chorionic plate inflammationWorth knowing
- rs7860896117,720,825A;Acommon in complete genomicsTypical
- rs10984447DBC1 · 119,222,275A;A>1.17x increased risk for multiple sclerosisWorth knowing
- rs10984561LOC105376250 · 119,496,299C;Ccommon in complete genomicsTypical
- rs4837752LOC105376253 · 120,294,359G;Gcommon in complete genomicsTypical
- rs1953126PHF19 · 120,878,222C;CnormalTypical
- rs3761847TRAF1 · 120,927,961G;G>1.32 x risk of rheumatoid arthritisWorth knowing
- rs10818488TRAF1 · 120,942,809A;A2.1x increased risk for rheumatoid arthritisTypical
- rs2300929C5 · 120,954,562T;Tcommon in complete genomicsTypical
- rs10985112C5 · 120,969,130G;Gcommon in complete genomicsTypical
- rs17611C5 · 121,006,922C;Ccommon in clinvarTypical
- rs25681C5 · 121,017,727G;Gcommon in clinvarTypical
- rs9408926CNTRL · 121,152,596C;Ccommon on affy axiom dataTypical
- rs9408928RAB14 · 121,189,639T;TNo summary available.Typical
- rs7042542DAB2IP · 121,565,769T;Tcommon in complete genomicsTypical
- rs7025486DAB2IP · 121,660,124A;Aslight (1.4x) increase in risk for abdominal aortic aneurysm and other vascular disordersMinor
- rs1571801DAB2IP · 121,665,094T;T>1.36x risk for prostate cancerMinor
- rs35061590DAB2IP · 121,713,734G;Gcommon genotypeTypical
- rs13290547DAB2IP · 121,725,216C;Ccommon in complete genomicsTypical
- rs3747851DAB2IP · 121,758,981G;Gcommon genotypeTypical
- rs10306114PTGS1 · 122,370,243A;GHigher risk of bleeding during coronary angiography?Minor
- rs3842787PTGS1 · 122,371,228T;THigher risk of bleeding during coronary angiographyImportant
- rs3842788PTGS1 · 122,377,927G;Gcommon in complete genomicsTypical
- rs3842789PTGS1 · 122,377,962G;Gcommon in complete genomicsTypical
- rs3842792PTGS1 · 122,381,428A;Acommon in complete genomicsTypical
- rs5789PTGS1 · 122,381,694C;Ccommon in complete genomicsTypical
- rs2808415CRB2 · 123,363,039A;Acommon in complete genomicsTypical
- rs872863DENND1A · 123,392,075C;CNo summary available.Typical
- rs7037102DENND1A · 123,555,360G;Gcommon in complete genomicsTypical
- rs10818854DENND1A · 123,684,499G;Gcommon on affy axiom dataTypical
- rs1110061NR5A1 · 124,500,523C;Ccommon in clinvarTypical
- rs10114038NR6A1 · 124,565,484A;Acommon genotypeTypical
- rs583134GOLGA1 · 124,911,921C;Ccommon in complete genomicsTypical
- rs430397HSPA5 · 125,238,840C;CNo summary available.Typical
- rs10986769MAPKAP1 · 125,460,061A;Acommon in complete genomicsTypical
- rs7854658LMX1B · 126,652,659G;Gcommon in complete genomicsTypical
- rs10987386LMX1B · 126,654,038T;TNo summary available.Typical
- rs10733682LMX1B · 126,698,635A;Acommon in clinvarTypical
- rs11545664ENG · 127,843,106C;Ccommon in clinvarTypical
- rs10987883SLC25A25-AS1 · 128,118,550A;Acommon in complete genomicsTypical
- rs13283456PTGES2 · 128,122,474C;Ccommon in complete genomicsTypical
- rs884115PTGES2 · 128,125,577C;Ccommon in complete genomicsTypical
- rs3003609DNM1 · 128,222,476C;CnormalTypical
- rs80358233TOR1A · 129,814,065-;-Torsion dystoniaVery important
- rs1801968TOR1A · 129,818,622C;Ccommon in clinvarTypical
- rs2296793TOR1A · 129,822,779G;Gcommon in clinvarTypical
- rs7024934NCS1 · 130,205,009A;ANo summary available.Typical
- rs2855192ABL1 · 130,852,664G;Gcommon in complete genomicsTypical
- rs10901296130,890,269G;Gcommon genotypeTypical
- rs103612NUP214 · 131,144,705C;TNo summary available.Typical
- rs2296949POMT1 · 131,510,049A;Acommon in clinvarTypical
- rs4740283131,572,909A;ANo summary available.Typical
- rs11243676NTNG2 · 132,221,380G;Gcommon on affy axiom dataTypical
- rs118203657TSC1 · 132,903,665A;GClassified as benign in ClinVarMinor
- rs2905072GFI1B · 132,969,648A;Acommon in complete genomicsTypical
- rs8176750ABO · 133,255,672G;Gcommon in complete genomicsTypical
- rs8176749ABO · 133,255,801C;CNo summary available.Typical
- rs8176747ABO · 133,255,928C;Ccommon in clinvarTypical
- rs8176746ABO · 133,255,935T;TType B blood group (of ABO system)Typical
- rs8176743ABO · 133,256,028C;CNo summary available.Typical
- rs8176740ABO · 133,256,085A;ANo summary available.Typical
- rs7853989ABO · 133,256,205C;CLikely blood group BTypical
- rs55964869ABO · 133,256,233G;Gcommon in complete genomicsTypical
- rs8176719ABO · 133,257,521-;-likely to be of blood type OTypical
- rs1008708453ABO · 133,262,144A;AO2 alleles (ABO Type O) may be presentWorth knowing
- rs657152ABO · 133,263,862A;AA few different minor risk associations; see detailsWorth knowing
- rs2519093ABO · 133,266,456C;Ccommon/normalTypical
- rs505922ABO · 133,273,813C;Cblood type is not O, increased risk for some diseases.Worth knowing
- rs495828133,279,294G;Gcommon/normalTypical
- rs2301612ADAMTS13 · 133,436,862C;Ccommon in clinvarTypical
- rs28647808ADAMTS13 · 133,440,409C;Camong diabetic patients, somewhat lower risk for complications but also lower response to therapyMinor
- rs3025343133,613,233G;Gcommon on affy axiom dataTypical
- rs1611115DBH · 133,635,393C;CnormalTypical
- rs2007153DBH · 133,638,697T;Tdecreased risk of schizophrenia in limited studyMinor
- rs1108580DBH · 133,639,992A;Acommon in clinvarTypical
- rs5320DBH · 133,642,351G;Gcommon in complete genomicsTypical
- rs4531DBH · 133,644,248G;Gcommon on affy axiom dataTypical
- rs2283123DBH · 133,650,175C;Cnormal risk of schizophrenia in limited studyMinor
- rs77905DBH · 133,652,975A;Acommon in clinvarTypical
- rs6271DBH · 133,657,152C;Ccommon in clinvarTypical
- rs129882DBH · 133,658,547C;Ccommon in clinvarTypical
- rs1805352RXRA · 134,408,103A;ANo summary available.Typical
- rs3118536RXRA · 134,416,616C;CNo summary available.Typical
- rs3118523134,443,675A;ANo summary available.Typical
- rs61735045COL5A1 · 134,750,808A;Alikely to be a benign variantMinor
- rs12722LOC101448202 · 134,842,570C;Ccommon in clinvarTypical
- rs7851696FCN2 · 134,887,245G;GNo summary available.Typical
- rs1537415GLT6D1 · 135,637,876C;C2x increased risk for periodontitisWorth knowing
- rs10781499CARD9 · 136,371,953G;Gcommon in clinvarTypical
- rs4077515CARD9 · 136,372,044C;Ccommon in clinvarTypical
- rs41309764NOTCH1 · 136,508,238A;GCongenital heart disease and valve calcification likelyVery important
- rs908832ABCA2 · 137,018,032A;A3.8x increased risk for early-onset AlzheimersTypical
No matches.
Source and license
Adapted from SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.