Chromosome 2
560 well-documented SNPs on chromosome 2, in order of position (GRCh38).
- rs11542478FAM110C · 38,938A;Acommon on affy axiom dataTypical
- rs3828329FAM150B · 279,705C;Tcommon in complete genomicsTypical
- rs2867125622,827C;CNo summary available.Typical
- rs6548238634,905C;CNo summary available.Typical
- rs2071403TPO · 1,413,472A;Acommon in clinvarTypical
- rs732609TPO · 1,496,155A;Acommon in clinvarTypical
- rs168641705,767,748T;Tcommon in complete genomicsTypical
- rs46692267,913,466A;ANo summary available.Typical
- rs35927125KLF11 · 10,046,292A;Acommon in clinvarTypical
- rs16857178FLJ33534 · 11,117,379G;Gcommon genotypeTypical
- rs10192566LPIN1 · 11,750,302C;Cif diabetic, poorer response to rosiglitazoneTypical
- rs10495584LPIN1 · 11,819,857G;GLowers men's blood pressure by -6.3/-3.8 mm Hg.Worth knowing
- rs11524LPIN1 · 11,826,191T;Tcommon in clinvarTypical
- rs1760556211,897,053C;Ccommon in complete genomicsTypical
- rs402713211,897,366A;A1.51x increased risk of developing bipolar disorderWorth knowing
- rs10929808MIR3681HG · 12,428,870A;Acommon in complete genomicsTypical
- rs1018049612,828,774A;GDental cariesTypical
- rs16861531LINC00276 · 14,257,928G;Gcommon in complete genomicsTypical
- rs156828214,926,053C;Ccommon in complete genomicsTypical
- rs7581919NBAS · 15,524,632T;Tcommon on affy axiom dataTypical
- rs643173115,722,878T;Tcommon in complete genomicsTypical
- rs758689815,821,475C;Ccommon in complete genomicsTypical
- rs1188933817,246,318G;Gcommon in complete genomicsTypical
- rs187604018,953,470A;Acommon in complete genomicsTypical
- rs4971516LDAH · 20,703,255T;Tcommon on affy axiom dataTypical
- rs756932820,901,018C;Ccommon in complete genomicsTypical
- rs675429520,983,311T;TNo summary available.Typical
- rs1042034APOB · 21,002,409C;Ccommon in clinvarTypical
- rs1042031APOB · 21,002,881T;TNo summary available.Typical
- rs12713559APOB · 21,006,196A;Gcarrier of possible familial hypercholesterolemia mutationImportant
- rs17241062APOB · 21,006,196G;GNo summary available.Typical
- rs5742904APOB · 21,006,288A;CFamilial HypercholesterolemiaVery important
- rs676210APOB · 21,008,652G;Gcommon in clinvarTypical
- rs6413458APOB · 21,008,720G;Gcommon in clinvarTypical
- rs693APOB · 21,009,323G;GnormalTypical
- rs568413APOB · 21,012,603C;Ccommon in complete genomicsTypical
- rs679899APOB · 21,028,042G;Gcommon in clinvarTypical
- rs520354APOB · 21,036,740A;Aincreased risk in men for biliary conditionsWorth knowing
- rs1367117APOB · 21,041,028G;Gcommon in clinvarTypical
- rs7600502LOC105374322 · 22,074,131A;ANo summary available.Typical
- rs6707600ITSN2 · 24,298,897T;Tcommon in complete genomicsTypical
- rs1804645NCOA1 · 24,752,089C;Ccommon in complete genomicsTypical
- rs3769671POMC · 25,167,284A;Acommon in complete genomicsTypical
- rs13388915RAB10 · 26,049,733G;Gcommon in complete genomicsTypical
- rs142787485RAB10 · 26,135,287A;GPossibly lower odds (~0.65x) of developing Alzheimer's in individuals at higher risk for the disorderVery important
- rs6753473LOC105374334 · 26,303,551T;Tcommon genotypeTypical
- rs3795958DRC1 · 26,444,262A;Acommon in clinvarTypical
- rs13031859OTOF · 26,519,093G;Gcommon in clinvarTypical
- rs2289408MAPRE3 · 27,025,376C;Ccommon in complete genomicsTypical
- rs1058065EIF2B4 · 27,364,857G;Gcommon in clinvarTypical
- rs1260326GCKR · 27,508,073T;Tslightly higher risk for goutMinor
- rs780094GCKR · 27,518,370T;Tmetabolic consequencesTypical
- rs17006206SLC4A1AP · 27,684,606A;Acommon in complete genomicsTypical
- rs1670283ALK · 29,193,706C;Ccommon in complete genomicsTypical
- rs7577363ALK · 29,653,477A;A>1.37x riskTypical
- rs1000916GALNT14 · 31,091,689T;Tcommon in complete genomicsTypical
- rs6543610LOC107985861 · 31,153,788C;Ccommon genotypeTypical
- rs1366813XDH · 31,347,510T;Tcommon in clinvarTypical
- rs9332975SRD5A2 · 31,525,347T;Tcommon in clinvarTypical
- rs523349SRD5A2 · 31,580,636C;CNo summary available.Typical
- rs632148SRD5A2 · 31,580,962C;Ccommon in clinvarTypical
- rs542631LTBP1 · 33,076,880G;Gcommon genotypeTypical
- rs3769528LTBP1 · 33,246,125A;Acommon in complete genomicsTypical
- rs13385731RASGRP3 · 33,476,823T;Tcommon on affy axiom dataTypical
- rs2254958EIF2AK2 · 37,149,148G;G1.61x reported increased risk for Alzheimer's; however, see comments on main rs-pageMinor
- rs3770748QPCT · 37,368,382G;Gaverage risk?Typical
- rs467076637,713,399T;Tcommon in complete genomicsTypical
- rs17511102LOC105374465 · 37,733,470A;Acommon in complete genomicsTypical
- rs6741148FAM82A1 · 38,050,689T;Tcommon in complete genomicsTypical
- rs9341266LOC107985872 · 38,068,851G;Gcommon in complete genomicsTypical
- rs28936701CYP1B1 · 38,070,949A;GCarrier of a primary congenital glaucoma mutationImportant
- rs1800440CYP1B1 · 38,070,996T;Tcommon on affy axiom dataTypical
- rs1056837CYP1B1 · 38,071,007A;Acommon in clinvarTypical
- rs1056836CYP1B1 · 38,071,060C;C0.3x decreased risk for prostate cancerWorth knowing
- rs1056827CYP1B1 · 38,075,034C;Ccommon in clinvarTypical
- rs9282671CYP1B1 · 38,075,148T;Tsmall chance of slightly increasing risk for a form of glaucomaMinor
- rs6741892GALM · 38,689,828A;Acommon in complete genomicsTypical
- rs3099950MORN2 · 38,882,417G;Gcommon on affy axiom dataTypical
- rs271673439,720,581C;Ccommon in complete genomicsTypical
- rs672118139,888,556C;Ccommon genotypeTypical
- rs17025867SLC8A1 · 40,351,419G;Gcommon genotypeTypical
- rs1012620LOC105374497 · 40,761,921A;Acommon in complete genomicsTypical
- rs6732426THADA · 43,360,365C;Ccurlier hairWorth knowing
- rs13429458THADA · 43,411,699A;Acommon in complete genomicsTypical
- rs6720173DYNC2LI1 · 43,813,262G;Gcommon in clinvarTypical
- rs6756629ABCG5 · 43,837,951G;Gcommon in complete genomicsTypical
- rs3806471ABCG5 · 43,839,035T;Tcommon in clinvarTypical
- rs11887534ABCG8 · 43,839,108C;C7x increased risk for gallstonesImportant
- rs4148211LOC102725159 · 43,844,604A;Acommon in clinvarTypical
- rs41360247LOC102725159 · 43,846,517T;Tcommon in complete genomicsTypical
- rs4953023ABCG8 · 43,846,861G;Gcommon in complete genomicsTypical
- rs4245791ABCG8 · 43,847,292T;Tcommon/normalTypical
- rs4148217ABCG8 · 43,872,294C;Ccommon in clinvarTypical
- rs6544718ABCG8 · 43,877,786C;CNo summary available.Typical
- rs698761SLC3A1 · 44,320,435G;Gcommon in clinvarTypical
- rs13414205CAMKMT · 44,435,336C;CNo summary available.Typical
- rs3213787SRBD1 · 45,419,685A;Acommon in complete genomicsTypical
- rs1262328846,407,506G;Gcommon in complete genomicsTypical
- rs17540621TTC7A · 47,002,700G;Gcommon on affy axiom dataTypical
- rs1126497EPCAM · 47,373,967C;T1.4x increased risk for breast cancerMinor
- rs1421EPCAM · 47,386,731T;Tcommon in clinvarTypical
- rs17217772MSH2 · 47,410,107A;Acommon in clinvarTypical
- rs63750347MSH2 · 47,412,522C;TLynch syndrome, pathogenic mutationVery important
- rs193922376MSH2 · 47,414,421A;TLynch syndrome, pathogenic mutationVery important
- rs12476364MSH2 · 47,416,295A;GLynch syndrome, pathogenic mutationVery important
- rs4987188MSH2 · 47,416,318G;Gcommon in complete genomicsTypical
- rs3732183MSH2 · 47,466,820G;Gcommon in clinvarTypical
- rs63749831MSH2 · 47,475,051-;AATLynch syndrome, pathogenic mutationVery important
- rs63750875MSH2 · 47,475,171C;CLynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)Very important
- rs2303428MSH2 · 47,476,361T;Tcommon in clinvarTypical
- rs63749932MSH2 · 47,476,399C;TLynch syndrome; pathogenic mutationVery important
- rs1800932MSH6 · 47,790,942A;Acommon in clinvarTypical
- rs1800935MSH6 · 47,795,976T;Tcommon in clinvarTypical
- rs1800937MSH6 · 47,798,625A;CLynch syndrome, pathogenic mutationVery important
- rs2020908MSH6 · 47,799,169C;Ccommon in complete genomicsTypical
- rs2020912MSH6 · 47,800,616C;Tunclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)Worth knowing
- rs121912532LHCGR · 48,688,065C;Ccommon in clinvarTypical
- rs2293275LHCGR · 48,694,236T;Tcommon in clinvarTypical
- rs13405728LHCGR · 48,751,020A;Acommon in complete genomicsTypical
- rs759106448,950,462T;Tcommon on affy axiom dataTypical
- rs6166FSHR · 48,962,782C;CFemales slightly more likely to be sterileMinor
- rs6165FSHR · 48,963,902C;Ccommon in clinvarTypical
- rs1394205FSHR · 49,154,446C;Ccommon in clinvarTypical
- rs1045881NRXN1 · 49,921,834C;Ccommon in clinvarTypical
- rs2303298NRXN1 · 50,623,548G;Gcommon in complete genomicsTypical
- rs2024513NRXN1 · 50,924,881A;A1.7x higher risk for schizophrenia (among Han Chinese)Minor
- rs12623467NRXN1 · 50,997,951C;Ccommon in complete genomicsTypical
- rs17041183NRXN1 · 51,002,517G;Gcommon in complete genomicsTypical
- rs12467557NRXN1 · 51,015,132A;Acommon in complete genomicsTypical
- rs1206397LOC730100 · 51,440,601C;CNo summary available.Typical
- rs2063871LOC730100 · 51,710,713G;Gcommon in complete genomicsTypical
- rs11889995LOC730100 · 51,936,272C;Ccommon in complete genomicsTypical
- rs1340766253,555,422C;Ccommon genotypeTypical
- rs1559040ACYP2 · 54,120,613C;Ccommon on affy axiom dataTypical
- rs2589113CCDC88A · 55,289,187G;Gcommon genotypeTypical
- rs671654355,930,826A;Acommon in complete genomicsTypical
- rs1020316659,562,570C;Ccommon genotypeTypical
- rs11886868BCL11A · 60,493,111C;Ccommon in clinvarTypical
- rs4672457FAM161A · 61,839,792A;Acommon in clinvarTypical
- rs1086533162,324,337A;A1.4x higher risk for ankylosing spondylitisMinor
- rs721048EHBP1 · 62,904,596A;Aslightly increased prostate cancer riskMinor
- rs11683229C2orf86 · 63,369,701A;Acommon on affy axiom dataTypical
- rs7572857CEP68 · 65,069,664G;Gcommon on affy axiom dataTypical
- rs1457451LOC105369166 · 65,635,244G;GNo summary available.Typical
- rs6710341MEIS1 · 66,531,290G;GIncreased risk of developing restless legs syndromeWorth knowing
- rs12469063MEIS1 · 66,537,176G;GIncreased risk of developing restless legs syndromeWorth knowing
- rs2300478MEIS1 · 66,554,321G;G>1.7x risk for developing restless legs syndromeWorth knowing
- rs672442267,749,656C;Ccommon genotypeTypical
- rs9309413LOC102724389 · 68,343,640C;Clowest sphingomyelin valuesTypical
- rs425453568,971,256T;Tcommon in complete genomicsTypical
- rs4315565ANTXR1 · 69,060,811A;Acommon in complete genomicsTypical
- rs7577851AAK1 · 69,496,578C;Ccommon in complete genomicsTypical
- rs4984LOC105374794 · 70,673,271G;Gcommon in complete genomicsTypical
- rs3755351ADD2 · 70,747,758T;T>1.3x risk for hypertensionTypical
- rs2080391CD207 · 70,831,139C;Ccommon in complete genomicsTypical
- rs13383830CD207 · 70,831,175T;Tcommon in complete genomicsTypical
- rs2266917ATP6V1B1 · 70,942,575C;Tcommon in complete genomicsTypical
- rs13407355DYSF · 71,513,823C;Ccommon genotypeTypical
- rs2303603DYSF · 71,600,724G;Gcommon in clinvarTypical
- rs6705628TET3 · 73,981,235C;Ccommon genotypeTypical
- rs10177833SLC4A5 · 74,230,591C;Cpossible reduction in risk for salt-induced hypertensionWorth knowing
- rs7571842SLC4A5 · 74,233,777G;Gpossible reduction in risk for salt-induced hypertensionWorth knowing
- rs3771829TACR1 · 75,137,019C;Ccommon/normalTypical
- rs115839275,483,619G;Gcommon in complete genomicsTypical
- rs17011455EVA1A · 75,563,363T;Tcommon genotypeTypical
- rs17011478EVA1A · 75,565,017C;Ccommon genotypeTypical
- rs6738962CTNNA2 · 80,054,047A;Acommon genotypeTypical
- rs1446109CTNNA2 · 80,311,294A;ANo summary available.Typical
- rs1049626581,441,684T;Tcommon on affy axiom dataTypical
- rs10496262LOC102724542 · 81,524,000C;CNo summary available.Typical
- rs1702244482,802,345C;Ccommon in complete genomicsTypical
- rs1339884884,018,044A;Acommon in complete genomicsTypical
- rs2028898GGCX · 85,550,147G;Gcommon/normalTypical
- rs11676382GGCX · 85,550,510C;Ccommon in clinvarTypical
- rs2592551GGCX · 85,553,008G;Gcommon in clinvarTypical
- rs699664GGCX · 85,553,413C;Ccommon in clinvarTypical
- rs1010VAMP8 · 85,581,859C;C1.75x risk of MIMinor
- rs7316SFTPB · 85,658,890T;Tcommon in complete genomicsTypical
- rs1130866SFTPB · 85,666,618G;GnormalTypical
- rs1138484ST3GAL5 · 85,861,188T;Tcommon in clinvarTypical
- rs165925888,360,069A;ANo summary available.Typical
- rs1805165LOC101928371 · 88,575,373C;Ccommon in clinvarTypical
- rs6750998EIF2AK3 · 88,583,424T;Tcommon in clinvarTypical
- rs867529EIF2AK3 · 88,613,755G;Gcommon in clinvarTypical
- rs232230IGKC · 88,857,435C;Ccommon in complete genomicsTypical
- rs2229169ADRA2B · 96,114,968T;T1.5x increased risk of heart attack and stroke but better emotional memory and stop-go performanceMinor
- rs2278206INPP4A · 98,555,781A;A1.16x increased risk for asthmaMinor
- rs7565981MBIP · 100,807,869G;Gcommon in complete genomicsTypical
- rs1811399NPAS2 · 100,862,552C;CNo summary available.Typical
- rs11123857NPAS2 · 100,987,350A;G1.44-fold increased risk of bipolar disorder or major depressionWorth knowing
- rs949963IL1R1 · 102,153,326C;Ccommon in complete genomicsTypical
- rs3771180IL1RL1 · 102,337,157G;Gcommon in complete genomicsTypical
- rs13431828IL1RL1 · 102,338,193C;Ccommon in complete genomicsTypical
- rs10197862IL1RL1 · 102,350,089A;Acommon in complete genomicsTypical
- rs2272127IL18RAP · 102,423,413C;CAssociated with herpes and schizophreniaMinor
- rs11465702IL18RAP · 102,441,432A;Acommon in complete genomicsTypical
- rs917997IL18RAP · 102,454,108C;CNo summary available.Typical
- rs12105421102,959,630C;Ccommon genotypeTypical
- rs11890236104,192,254T;TNo summary available.Typical
- rs7570682104,366,809A;A1.6x riskTypical
- rs17636747TGFBRAP1 · 105,261,413C;CNo summary available.Typical
- rs1669539105,998,818T;Tcommon genotypeTypical
- rs2219078SULT1C3 · 108,258,742G;GNo summary available.Typical
- rs3731685SULT1C4 · 108,387,198G;Gcommon in complete genomicsTypical
- rs3827760EDAR · 108,897,145G;Gstraighter, thicker hair, and increased odds of having shovel-shaped incisorsWorth knowing
- rs7578982ACOXL · 111,078,961C;Tcommon in complete genomicsTypical
- rs6720394MIR4435-2HG · 111,231,795T;Tcommon on affy axiom dataTypical
- rs7604639MERTK · 111,994,351G;Gcommon in clinvarTypical
- rs2230515MERTK · 111,997,424A;Acommon in clinvarTypical
- rs2048874CKAP2L · 112,766,390C;CNo summary available.Typical
- rs1800587IL1A · 112,785,383A;AIncreased waist circumference and a much greater risk of Intervertebral disc diseaseWorth knowing
- rs1143634IL1B · 112,832,813G;GnormalTypical
- rs1143627IL1B · 112,836,810G;Gcommon in clinvarTypical
- rs16944IL1B · 112,837,290A;AIncreased risk (~3x) for osteoarthritisWorth knowing
- rs315921IL1RN · 113,114,474G;GNo summary available.Typical
- rs419598IL1RN · 113,129,630C;C0.29x lower risk for periodontitisTypical
- rs315952IL1RN · 113,132,727T;Tcommon in clinvarTypical
- rs315951IL1RN · 113,133,009C;Ccommon in clinvarTypical
- rs4252041IL1RN · 113,133,033C;Ccommon in clinvarTypical
- rs9005IL1RN · 113,133,835G;Gcommon in complete genomicsTypical
- rs315946113,136,287G;GNo summary available.Typical
- rs1375144DPP10 · 115,483,610G;G1.59x increased risk of developing bipolar disorder (one study)Minor
- rs1446495DPP10 · 115,768,384A;Acommon in complete genomicsTypical
- rs17586756LOC107985940 · 118,072,882C;Ccommon in complete genomicsTypical
- rs10490626LOC107985940 · 118,078,265G;GNo summary available.Typical
- rs7566605LOC107985940 · 118,078,449C;Cmixed evidence of increased obesity risk, may suppress excercise effects in menTypical
- rs17047718LOC107985940 · 118,079,736A;Acommon in complete genomicsTypical
- rs17587100LOC107985940 · 118,080,834A;Acommon in complete genomicsTypical
- rs12464355INSIG2 · 118,092,274A;ANo summary available.Typical
- rs10490625INSIG2 · 118,101,980G;Gcommon in complete genomicsTypical
- rs10490624INSIG2 · 118,104,916T;Tcommon in complete genomicsTypical
- rs12623648INSIG2 · 118,112,002G;GNo summary available.Typical
- rs17009726MARCO · 118,967,884A;Acommon in complete genomicsTypical
- rs8192506DBI · 119,372,265A;Acommon in complete genomicsTypical
- rs7581710120,437,605A;Acommon in complete genomicsTypical
- rs3943552GLI2 · 120,824,482C;CNo summary available.Typical
- rs11122834GLI2 · 120,943,713C;Ccommon genotypeTypical
- rs3738880GLI2 · 120,989,380G;Gcommon in clinvarTypical
- rs17367118LOC105373595 · 122,884,035G;Gcommon on affy axiom dataTypical
- rs11899928CNTNAP5 · 124,499,159T;Tcommon genotypeTypical
- rs17727261CNTNAP5 · 124,524,333C;Ccommon in complete genomicsTypical
- rs6733840LOC101929926 · 126,902,405T;Tcommon in complete genomicsTypical
- rs13418717126,905,321T;Tcommon in complete genomicsTypical
- rs7561528LOC105373605 · 127,132,061G;Gcommon/normalTypical
- rs744373127,137,039G;G1.28x risk of Alzheimer'sWorth knowing
- rs4150403ERCC3 · 127,292,492C;CNo summary available.Typical
- rs1799810PROC · 127,418,464A;Acommon in clinvarTypical
- rs1401296LOC105373608 · 127,431,732C;TNo summary available.Typical
- rs17015535WDR33 · 127,745,011A;Acommon genotypeTypical
- rs13013415WDR33 · 127,762,223T;Tcommon genotypeTypical
- rs16831128132,386,819A;Acommon in complete genomicsTypical
- rs6722456133,771,520G;Gcommon genotypeTypical
- rs10198552ACMSD · 134,842,306T;Tcommon genotypeTypical
- rs16832011LCT · 135,787,729A;Acommon genotypeTypical
- rs2322659LCT · 135,798,089T;Tcommon in clinvarTypical
- rs4954449LCT · 135,817,964C;Ccommon in complete genomicsTypical
- rs4988235MCM6 · 135,851,076G;Glikely to be lactose intolerant as an adultWorth knowing
- rs41380347MCM6 · 135,851,081C;CLactase persistenceWorth knowing
- rs4988234MCM6 · 135,851,103C;Ccommon in complete genomicsTypical
- rs182549MCM6 · 135,859,184C;Cpossibly lactose intolerantWorth knowing
- rs2228014CXCR4 · 136,115,514G;Gcommon on affy axiom dataTypical
- rs934299136,581,370G;Gcommon in complete genomicsTypical
- rs17583889LOC107985948 · 137,988,469C;Ccommon/normalTypical
- rs11558538LOC107985948 · 138,002,079C;Ccommon on affy axiom dataTypical
- rs1399645LOC105373644 · 139,390,262C;Ccommon in complete genomicsTypical
- rs16842994139,869,162C;Ccommon genotypeTypical
- rs491391LRP1B · 140,604,489A;Acommon in complete genomicsTypical
- rs6711223ZEB2 · 144,400,257G;Gcommon in clinvarTypical
- rs7355746144,594,254C;CNo summary available.Typical
- rs10427255145,367,955C;Chighest odds of photic sneeze reflexWorth knowing
- rs2307394ORC4 · 147,958,859T;Tcommon in clinvarTypical
- rs6435387KIF5C · 149,008,736G;Gcommon genotypeTypical
- rs1012307LOC101929231 · 149,798,707A;Acommon genotypeTypical
- rs6716455LOC105373684 · 150,269,889G;Gcommon on affy axiom dataTypical
- rs7560163150,781,422C;Ccommon genotypeTypical
- rs10195263150,869,278A;ANo summary available.Typical
- rs6713162NEB · 151,640,012A;Acommon in clinvarTypical
- rs13013209NEB · 151,643,935C;CnormalTypical
- rs7426114NEB · 151,671,058C;TNo summary available.Typical
- rs6711382NEB · 151,674,563A;Acommon in clinvarTypical
- rs6735208NEB · 151,679,984A;ANo summary available.Typical
- rs17188434LINC01876 · 156,240,264T;Tcommon in complete genomicsTypical
- rs12803NR4A2 · 156,325,413A;Acommon in clinvarTypical
- rs295791LOC107985955 · 156,890,146C;Ccommon in complete genomicsTypical
- rs590551156,890,146C;CNo summary available.Typical
- rs16841722CYTIP · 157,421,701T;Tcommon in complete genomicsTypical
- rs3769376CYTIP · 157,421,733G;Gcommon in complete genomicsTypical
- rs1146031ACVR1 · 157,770,468T;Tcommon genotypeTypical
- rs12694937ACVR1 · 157,800,921T;Tcommon genotypeTypical
- rs2074955UPP2 · 158,121,282A;Acommon in complete genomicsTypical
- rs10497203TANC1 · 158,994,911A;Acommon in clinvarTypical
- rs7582141TANC1 · 159,042,977G;Gcommon in clinvarTypical
- rs6432512TANC1 · 159,043,401C;Ccommon in clinvarTypical
- rs264651TANC1 · 159,072,919A;Acommon in clinvarTypical
- rs264588TANC1 · 159,079,879C;Ccommon in clinvarTypical
- rs264631TANC1 · 159,094,353C;Ccommon in clinvarTypical
- rs13022357TANC1 · 159,213,245G;Gcommon in complete genomicsTypical
- rs4665058BAZ2B · 159,333,698A;A~4x increased risk among Europeans for sudden cardiac deathWorth knowing
- rs6718526RBMS1 · 160,357,664C;C1.9x risk of type-2 diabetesTypical
- rs10208407160,900,618G;Gcommon genotypeTypical
- rs3820998LOC105373719 · 161,138,615C;Ccommon in complete genomicsTypical
- rs2270447162,103,238T;Tcommon in complete genomicsTypical
- rs1990760IFIH1 · 162,267,541C;Ccommon in clinvarTypical
- rs3747517IFIH1 · 162,272,314T;Tcommon in clinvarTypical
- rs10930046IFIH1 · 162,281,473T;Tcommon genotypeTypical
- rs3788964GCA · 162,350,970A;ANo summary available.Typical
- rs17716942KCNH7 · 162,404,181T;Tcommon on affy axiom dataTypical
- rs10221833COBLL1 · 164,720,654G;Gcommon in complete genomicsTypical
- rs13424957LOC101929633 · 164,893,880C;Ccommon in complete genomicsTypical
- rs17183814SCN2A · 165,295,879G;Gcommon in complete genomicsTypical
- rs2304016SCN2A · 165,311,993A;Acommon in complete genomicsTypical
- rs16851009GALNT3 · 165,774,197C;Ccommon in complete genomicsTypical
- rs2298771SCN1A · 166,036,278C;Ccommon in clinvarTypical
- rs121917967SCN1A · 166,046,910A;TDravet syndrome and severe epileptic seizure syndrome(s) possibleVery important
- rs6746030LOC101929680 · 166,242,648A;AIncreased perception of painMinor
- rs4369876SCN9A · 166,272,746A;CPossibly somewhat more insensitive to pain (see discussion)Important
- rs12478318SCN9A · 166,277,030G;TPossibly somewhat more insensitive to pain (see discussion)Important
- rs73969684SCN9A · 166,305,834C;TPossible pain-related mutation, but, may be benignImportant
- rs4438497SCN9A · 166,320,849T;Tcommon genotypeTypical
- rs1061471STK39 · 167,954,842C;Ccommon in complete genomicsTypical
- rs3754777STK39 · 168,159,404T;Tslightly higher blood pressure if CaucasianMinor
- rs6749447STK39 · 168,184,876G;Gslightly higher blood pressure if CaucasianTypical
- rs2390669STK39 · 168,235,432A;Acommon in complete genomicsTypical
- rs9917256168,286,525G;Gcommon in complete genomicsTypical
- rs573225G6PC2 · 168,901,031G;GnormalTypical
- rs560887G6PC2 · 168,906,638C;CAvg. fasting Plasma Glucose 5.18 mmol/L (93 mg/dl).Worth knowing
- rs16856187168,913,876A;Acommon in complete genomicsTypical
- rs16856247ABCB11 · 168,927,903C;Ccommon in complete genomicsTypical
- rs497692ABCB11 · 168,932,506T;Tcommon in clinvarTypical
- rs2287622ABCB11 · 168,973,818G;G2.8x higher risk for intrahepatic cholestasis of pregnancyTypical
- rs16856332ABCB11 · 168,984,064T;TNo summary available.Typical
- rs11568372ABCB11 · 168,990,819T;Tcommon in clinvarTypical
- rs2287616ABCB11 · 168,990,902A;Acommon in clinvarTypical
- rs11568377ABCB11 · 168,996,710G;Gcommon in clinvarTypical
- rs3815676ABCB11 · 169,013,869T;TNo summary available.Typical
- rs2075252LRP2 · 169,154,475T;Tcommon in clinvarTypical
- rs17848169LRP2 · 169,204,093T;Tcommon in clinvarTypical
- rs3749034GAD1 · 170,816,965G;Gcommon in clinvarTypical
- rs3828275GAD1 · 170,826,230C;Ccommon/normalTypical
- rs769407GAD1 · 170,837,198G;Gcommon/normalTypical
- rs4668338170,876,715C;Ccommon in complete genomicsTypical
- rs2292813SLC25A12 · 171,787,719C;Tdecreased risk of autismWorth knowing
- rs2056202SLC25A12 · 171,855,970C;Ccommon but increased risk of autismWorth knowing
- rs2141698ITGA6 · 172,425,667C;Ccommon in complete genomicsTypical
- rs10207654ITGA6 · 172,443,028A;Acommon in complete genomicsTypical
- rs12621278ITGA6 · 172,446,825A;Acommon in complete genomicsTypical
- rs11895564LOC101929947 · 172,475,080A;GNo summary available.Typical
- rs6433379RAPGEF4 · 172,755,737A;Acommon in complete genomicsTypical
- rs2676527RAPGEF4 · 172,882,984G;Gcommon in complete genomicsTypical
- rs7590983173,497,621T;TNo summary available.Typical
- rs185584ATP5G3 · 175,176,702A;Acommon/normalTypical
- rs4972755175,375,121G;Gcommon in complete genomicsTypical
- rs13418078HOXD4 · 176,151,087C;Ccommon in complete genomicsTypical
- rs2072590HAGLR · 176,177,905A;A1.4x increased risk for ovarian cancerMinor
- rs2588882HNRNPA3 · 177,222,437T;Tcommon in complete genomicsTypical
- rs2001350NFE2L2 · 177,235,697T;Tcommon in complete genomicsTypical
- rs1962142NFE2L2 · 177,248,756G;Gcommon in complete genomicsTypical
- rs7580640OSBPL6 · 178,383,693C;Ccommon genotypeTypical
- rs2555818TTN · 178,546,299A;Acommon in clinvarTypical
- rs16866412TTN · 178,609,941G;Gcommon in clinvarTypical
- rs2244492TTN · 178,689,578C;Ccommon in clinvarTypical
- rs17355446TTN · 178,724,514G;Gcommon in complete genomicsTypical
- rs4893853TTN · 178,767,769T;Tcommon genotypeTypical
- rs12476289TTN · 178,777,248C;Ccommon in complete genomicsTypical
- rs16867321180,497,652C;Ccommon in complete genomicsTypical
- rs918959180,649,002G;Gcommon in complete genomicsTypical
- rs12988934ITGA4 · 181,458,938C;Ccommon on affy axiom dataTypical
- rs155100ITGA4 · 181,485,360A;Tcommon in complete genomicsTypical
- rs7775FRZB · 182,834,857G;GNo summary available.Typical
- rs288326FRZB · 182,838,608G;Gcommon in complete genomicsTypical
- rs1344706ZNF804A · 184,913,701A;A1.2x increased risk for schizophreniaMinor
- rs3738919ITGAV · 186,656,533C;C1.94x risk of developing rheumatoid arthritisWorth knowing
- rs5940TFPI · 187,466,977C;CNo summary available.Typical
- rs1800255COL3A1 · 188,999,354A;Aincreased risk for pelvic organ prolapseWorth knowing
- rs587779540COL3A1 · 189,006,418G;Gcommon in clinvarTypical
- rs1516446COL3A1 · 189,010,695G;Gcommon in complete genomicsTypical
- rs11568350SLC40A1 · 189,565,370C;Ccommon in complete genomicsTypical
- rs12053254ANKAR · 189,742,427T;Tcommon genotypeTypical
- rs7606224ORMDL1 · 189,778,923C;Ccommon genotypeTypical
- rs5742933PMS1 · 189,784,590G;Gcommon in clinvarTypical
- rs5743030PMS1 · 189,813,819G;GNo summary available.Typical
- rs1805086MSTN · 190,060,351T;Tcommon on affy axiom dataTypical
- rs10931468NAB1 · 190,673,836C;Ccommon in complete genomicsTypical
- rs3024908LOC105373805 · 191,029,415T;Tcommon in complete genomicsTypical
- rs3821236STAT4 · 191,038,032A;A2x higher risk of lupusWorth knowing
- rs3024866STAT4 · 191,058,115G;Gcommon in clinvarTypical
- rs10168266STAT4 · 191,071,078C;Cnormal risk of Sjogren's syndromeTypical
- rs7574865STAT4 · 191,099,907T;T1.69x risk of rheumatoid arthritis; 2.4x risk of SLE; 2.28x risk of Sjögren's syndrome; increased risk of type-1 diabetes; and increased risk of primary biliary cirrhosis.Important
- rs10181656STAT4 · 191,105,153G;G1.7x increased SLE riskWorth knowing
- rs7582694STAT4 · 191,105,394C;C1.71x increased SLE riskTypical
- rs10497721TMEFF2 · 192,049,636C;Ccommon on affy axiom dataTypical
- rs13007495TMEFF2 · 192,090,779T;Tcommon on affy axiom dataTypical
- rs17662626LOC107985969 · 193,119,895A;Acommon in complete genomicsTypical
- rs801350194,682,669A;Acommon genotypeTypical
- rs801378194,695,273C;Ccommon genotypeTypical
- rs788016HSPD1 · 197,487,569A;GNo summary available.Typical
- rs700651BOLL · 197,766,990G;G~1.23x increased risk of intracranial aneurysmWorth knowing
- rs7595412PLCL1 · 198,097,519A;Acommon on affy axiom dataTypical
- rs988583PLCL1 · 198,123,211C;Ccommon in complete genomicsTypical
- rs2054125LOC105373831 · 198,520,997C;Ccommon genotypeTypical
- rs16830366LOC105373831 · 198,720,832C;Ccommon genotypeTypical
- rs10497845200,033,174T;TNo summary available.Typical
- rs13430864AOX3P-AOX2P · 200,783,916T;Tcommon genotypeTypical
- rs719126CFLAR · 201,153,107C;Ccommon in complete genomicsTypical
- rs3900115CASP10 · 201,185,954A;Acommon in clinvarTypical
- rs13010627CASP10 · 201,209,375G;Gcommon in clinvarTypical
- rs17860404CASP10 · 201,209,375G;GNo summary available.Typical
- rs13006529CASP10 · 201,217,736T;Tcommon in clinvarTypical
- rs3834129CASP8 · 201,232,809-;CTTACTSlightly decreased risk (0.9x) of certain cancersMinor
- rs2037815CASP8 · 201,236,992A;Gcommon in complete genomicsTypical
- rs6704688CASP8 · 201,241,309C;Tcommon in complete genomicsTypical
- rs3769823CASP8 · 201,258,272A;Acommon in clinvarTypical
- rs3817578CASP8 · 201,271,872C;Ccommon in complete genomicsTypical
- rs1045485CASP8 · 201,284,866C;CReduced Risk of Breast CancerWorth knowing
- rs17468277ALS2CR12 · 201,289,477C;Ccommon in clinvarTypical
- rs3219156ALS2 · 201,760,892C;Ccommon in clinvarTypical
- rs17385675201,942,473C;Ccommon in complete genomicsTypical
- rs1521882KIAA2012 · 202,085,128A;Acommon in complete genomicsTypical
- rs863223423BMPR2 · 202,464,918-;APulmonary arterial hypertensionVery important
- rs1061157BMPR2 · 202,556,476G;Gcommon in clinvarTypical
- rs6725887WDR12 · 202,881,162T;TNo summary available.Typical
- rs11888559CYP20A1 · 203,300,448C;Ccommon in complete genomicsTypical
- rs733618CTLA4 · 203,866,221C;T1.87x risk for myasthenia gravisMinor
- rs4553808CTLA4 · 203,866,282A;AnormalTypical
- rs5742909CTLA4 · 203,867,624C;CNo summary available.Typical
- rs231775CTLA4 · 203,867,991G;G2.3x risk of Hashimoto's thyroiditis, 1.47x risk of Graves' diseaseWorth knowing
- rs231778CTLA4 · 203,869,098A;Acommon in complete genomicsTypical
- rs3087243CTLA4 · 203,874,196A;Gincreased risk for auto-immune diseasesMinor
- rs11571323ICOS · 203,954,121G;Gcommon in complete genomicsTypical
- rs10183087ICOS · 203,959,601A;Acommon in clinvarTypical
- rs4404254ICOS · 203,960,563T;Tcommon in clinvarTypical
- rs10932037ICOS · 203,960,623C;Ccommon in clinvarTypical
- rs1559931ICOS · 203,961,006G;Gcommon in clinvarTypical
- rs4675379ICOS · 203,961,372G;Gcommon in complete genomicsTypical
- rs4673301204,503,735T;Tcommon genotypeTypical
- rs2335704PARD3B · 205,000,109A;Acommon in complete genomicsTypical
- rs1207421PARD3B · 205,285,870G;Gcommon on affy axiom dataTypical
- rs1801318NDUFS1 · 206,141,952T;Tcommon in clinvarTypical
- rs2277912FASTKD2 · 206,769,512T;Tcommon on affy axiom dataTypical
- rs7594645FASTKD2 · 206,781,950G;Gslightly better memory performance in older adultsWorth knowing
- rs7568369KLF7 · 207,166,591G;T0.90x reduced risk of obesityMinor
- rs16839883CREB1 · 207,564,618A;Acommon genotypeTypical
- rs7569963METTL21A · 207,608,460G;GNo summary available.Typical
- rs2952768207,629,510C;Cless drug dependence, decreased effectiveness of analgesicsMinor
- rs28931604CRYGC · 208,128,226G;Gcommon in clinvarTypical
- rs2286963ACADL · 210,195,326T;Tcommon in clinvarTypical
- rs3764913ACADL · 210,210,185T;Tcommon in clinvarTypical
- rs715CPS1 · 210,678,331T;Tcommon in clinvarTypical
- rs2216405210,752,170A;Acommon in complete genomicsTypical
- rs3748960ERBB4 · 211,383,109T;Tcommon genotypeTypical
- rs7598440ERBB4 · 211,928,473C;TNo summary available.Typical
- rs707284ERBB4 · 211,974,321A;GNo summary available.Typical
- rs12619285LOC102725082 · 212,959,321A;Acommon in complete genomicsTypical
- rs28997576BARD1 · 214,752,454G;Gprobably increased risk of breast cancerWorth knowing
- rs3768716BARD1 · 214,771,070T;TnormalTypical
- rs2229571BARD1 · 214,780,740C;Ccommon in clinvarTypical
- rs6435862BARD1 · 214,807,822G;G2.8x higher risk of aggressive neuroblastomaWorth knowing
- rs1048108LOC101928103 · 214,809,500G;Gcommon in clinvarTypical
- rs726070LOC101928103 · 214,948,607T;TTwo copies of a variant now thought likely to benignMinor
- rs7560008ABCA12 · 215,011,442A;Acommon in clinvarTypical
- rs11891778ABCA12 · 215,045,850G;Gcommon in clinvarTypical
- rs4673993ATIC · 215,347,616T;Tcommon in clinvarTypical
- rs6707530FN1 · 215,375,861G;Gin colorectal cancer, may allow cancer cells to invade deeper layersMinor
- rs1250204FN1 · 215,379,109C;Ccommon in complete genomicsTypical
- rs17458018FN1 · 215,420,652T;Tcommon genotypeTypical
- rs7590720PECR · 216,033,935A;Acommon/normalTypical
- rs828907XRCC5 · 216,108,009G;TSlightly increased risk of bladder cancer and 2x risk of developing bladder cancer in smokersWorth knowing
- rs9288516XRCC5 · 216,188,541A;A2x higher risk for hepatocellular cancerWorth knowing
- rs10169372LOC101928278 · 217,006,626A;Acommon in complete genomicsTypical
- rs13387042LOC105373874 · 217,041,109A;A1.24x increased risk for breast cancerMinor
- rs966423DIRC3 · 217,445,617C;CPossible elevated thyroid cancer riskWorth knowing
- rs6435999DIRC3 · 217,658,439A;Acommon in complete genomicsTypical
- rs2854386CXCR1 · 218,162,779C;Ccommon in complete genomicsTypical
- rs2234671CXCR1 · 218,164,385C;Ccommon in complete genomicsTypical
- rs16858811CXCR1 · 218,165,120A;Acommon in complete genomicsTypical
- rs3138060CXCR1 · 218,166,777G;Gcommon in complete genomicsTypical
- rs13403276ARPC2 · 218,216,574T;TNo summary available.Typical
- rs6733051ARPC2 · 218,219,810C;Ccommon genotypeTypical
- rs3731863SLC11A1 · 218,387,485C;Ccommon in complete genomicsTypical
- rs17235409SLC11A1 · 218,395,009G;Gcommon in complete genomicsTypical
- rs17235416SLC11A1 · 218,395,091I;Icommon genotypeTypical
- rs7349332WNT10A · 218,891,661T;Thair curlWorth knowing
- rs359980218,964,484T;Tcommon genotypeTypical
- rs359965SNHG9 · 218,976,169G;Gcommon in complete genomicsTypical
- rs1052483219,069,626G;Gcommon in complete genomicsTypical
- rs6724465NHEJ1 · 219,079,124G;Gcommon in complete genomicsTypical
- rs16859517NHEJ1 · 219,084,462C;Ccommon in complete genomicsTypical
- rs2059693INHA · 219,577,768T;T1.6x increased risk for testicular cancerMinor
- rs17348202221,207,458T;TNo summary available.Typical
- rs2855268PAX3 · 222,202,200C;Ccommon in clinvarTypical
- rs1440072223,072,020T;Tcommon on affy axiom dataTypical
- rs16864755LOC100289013 · 223,409,904G;Gcommon in complete genomicsTypical
- rs16864968SCG2 · 223,594,965A;Acommon in complete genomicsTypical
- rs975278SERPINE2 · 223,982,990T;T1.5x higher risk for emphysema, higher in smokersMinor
- rs2943634226,203,364A;Alower risk of ischemic strokeWorth knowing
- rs2943641226,229,029C;Cincreased risk for type 2 diabetesTypical
- rs1801278IRS1 · 226,795,828T;Treduced colorectal risk when combined with INSR SNPTypical
- rs10178458COL4A3 · 227,246,719C;TNo summary available.Typical
- rs6436669COL4A3 · 227,248,459A;Acommon in clinvarTypical
- rs11677877COL4A3 · 227,266,453A;Acommon on affy axiom dataTypical
- rs11890081DNER · 229,485,273T;Tcommon genotypeTypical
- rs1135791SP110 · 230,177,560A;Acommon in clinvarTypical
- rs3948464SP110 · 230,185,999G;GNo summary available.Typical
- rs2114592SP110 · 230,210,491G;Gcommon in clinvarTypical
- rs1063154SP110 · 230,212,386A;Acommon in complete genomicsTypical
- rs9061SP110 · 230,212,395C;Ccommon in clinvarTypical
- rs11556887SP110 · 230,212,961G;Gcommon in clinvarTypical
- rs1346311SP110 · 230,217,672G;Gcommon in complete genomicsTypical
- rs4972946SP140 · 230,284,393A;Acommon on affy axiom dataTypical
- rs17275498230,555,686A;Acommon on affy axiom dataTypical
- rs79874540HTR2B · 231,123,707A;G2-3 fold higher risk of impulsive/aggressive behaviour when drunkImportant
- rs16828074LOC100996253 · 231,454,043C;Ccommon genotypeTypical
- rs749052231,931,900T;Tcommon on affy axiom dataTypical
- rs7571816DIS3L2 · 232,212,354A;Acommon in complete genomicsTypical
- rs1130335ALPP · 232,378,876C;Ccommon in clinvarTypical
- rs10210302ATG16L1 · 233,250,193T;T1.8x increased risk for Crohn's diseaseMinor
- rs2241880ATG16L1 · 233,274,722G;G2x-3x increased risk for Crohn's disease in CaucasiansWorth knowing
- rs753107507SAG · 233,327,125G;TRetinitis pigmentosa likelyVery important
- rs1046974SAG · 233,346,901G;Gcommon in clinvarTypical
- rs6704644USP40 · 233,498,009G;Gcommon in complete genomicsTypical
- rs13394720233,593,475T;Tcommon on affy axiom dataTypical
- rs17863762UGT1A8 · 233,618,537G;Gcommon in complete genomicsTypical
- rs11892031UGT1A10 · 233,656,637A;ANo summary available.Typical
- rs17863783UGT1A6 · 233,693,631G;Gcommon in complete genomicsTypical
- rs3755319UGT1A10 · 233,758,936C;Cmost likely a benign polymorphismMinor
- rs887829UGT1A10 · 233,759,924T;THigher levels of serum bilirubin, associated with lower risk for coronary artery diseaseWorth knowing
- rs34983651UGT1A10 · 233,760,233-;-normalTypical
- rs34815109UGT1A10 · 233,760,234-;-normalTypical
- rs4148323UGT1A1 · 233,760,498A;Ahomozygous for UGT1A1*6Typical
- rs6742078UGT1A10 · 233,763,993T;T+16% bilirubin levels increased risk of gallstonesWorth knowing
- rs1042640MROH2A · 233,772,898G;Gcommon in clinvarTypical
- rs8330MROH2A · 233,772,999G;Gcommon in clinvarTypical
- rs2361502HEATR7B1 · 233,790,144C;CPossible higher levels of serum bilirubin and lower risk for coronary artery diseaseMinor
- rs579327233,859,421C;Ccommon in complete genomicsTypical
- rs10187654233,905,414C;Ccommon in complete genomicsTypical
- rs10166942TRPM8 · 233,916,448C;C0.7x lower risk for migrainesMinor
- rs12472151TRPM8 · 233,944,048G;Gcommon genotypeTypical
- rs11562975TRPM8 · 233,945,906G;Gcommon in complete genomicsTypical
- rs2042831LOC105373938 · 234,948,470G;Gcommon in complete genomicsTypical
- rs1131296COL6A3 · 237,334,649G;Gcommon in clinvarTypical
- rs2270669COL6A3 · 237,334,821C;Ccommon in clinvarTypical
- rs3820808LRRFIP1 · 237,739,162C;Ccommon in complete genomicsTypical
- rs11689421LRRFIP1 · 237,742,046T;Tcommon in complete genomicsTypical
- rs7575941LRRFIP1 · 237,758,405G;Gcommon in complete genomicsTypical
- rs3769053LRRFIP1 · 237,762,149T;Tcommon in complete genomicsTypical
- rs3806505LRRFIP1 · 237,767,806A;Acommon in complete genomicsTypical
- rs6739130LRRFIP1 · 237,780,726A;Acommon in complete genomicsTypical
- rs11686141LRRFIP1 · 237,780,915A;Acommon in complete genomicsTypical
- rs3769048RAMP1 · 237,861,218G;Gcommon in complete genomicsTypical
- rs11689432LOC643387 · 238,232,864G;Gcommon in clinvarTypical
- rs121908635PER2 · 238,257,003C;TMorning Lark (people waking up very early)Very important
- rs3739070TRAF3IP1 · 238,397,627A;Acommon in complete genomicsTypical
- rs6707013LINC01940 · 238,921,914G;Gcommon in complete genomicsTypical
- rs12477314238,955,452C;Ccommon in complete genomicsTypical
- rs13424612NDUFA10 · 239,960,704C;Ccommon in clinvarTypical
- rs2953145RNPEPL1 · 240,576,179G;GnormalTypical
- rs2975766CAPN10 · 240,598,657G;Gcommon in complete genomicsTypical
- rs3749172GPR35 · 240,630,832A;A>1.45x Increased risk for Crohn's disease in KoreansTypical
- rs4426527AGXT · 240,878,099A;Acommon in clinvarTypical
- rs2227982LOC105373977 · 241,851,281G;Gcommon genotypeTypical
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.