Chromosome 6
653 well-documented SNPs on chromosome 6, in order of position (GRCh38).
- rs9501753221,146G;Gcommon genotypeTypical
- rs6927090252,145G;Gcommon genotypeTypical
- rs1033180383,546C;Ccommon in complete genomicsTypical
- rs12203592IRF4 · 396,321C;TPrimarily in Europeans; likely presence of freckles, brown hair and high sensitivity of skin to sun exposure.Worth knowing
- rs872071IRF4 · 411,064A;G~1.5x increased risk for chronic lymphocytic leukemiaMinor
- rs1540771LOC105374875 · 466,033T;Tcommon in complete genomicsTypical
- rs12210050LOC105374875 · 475,489C;TSlightly higher risk for basal cell carcinomaMinor
- rs116446171484,453C;GSignificantly increased (~20x) risk for a rare B-cell lymphomaVery important
- rs9378688GMDS · 2,235,399G;Gcommon on affy axiom dataTypical
- rs4959235SLC22A23 · 3,359,103C;Ccommon in complete genomicsTypical
- rs6942328LOC105374894 · 4,512,745T;Tcommon in complete genomicsTypical
- rs2224391LYRM4 · 5,260,703A;Acommon in clinvarTypical
- rs1050783F13A1 · 6,145,459C;Ccommon in clinvarTypical
- rs5988F13A1 · 6,151,904C;Ccommon in clinvarTypical
- rs5987F13A1 · 6,151,907C;Ccommon in complete genomicsTypical
- rs2815822F13A1 · 6,320,575G;Gcommon/normalTypical
- rs1334710LY86-AS1 · 6,583,488A;AaverageTypical
- rs977785LY86 · 6,588,648A;AaverageTypical
- rs7740529LY86 · 6,610,376C;Ccommon in complete genomicsTypical
- rs2326810LY86 · 6,612,234G;Gcommon in complete genomicsTypical
- rs2076295DSP · 7,562,999G;GSlightly increased risk for pulmonary fibrosis (and decreased DSP expression)Minor
- rs28931610DSP · 7,584,358T;Tcarrier of a skin fragility/woolly hair syndrome alleleVery important
- rs9505298BMP6 · 7,881,216G;Gcommon in complete genomicsTypical
- rs2277105BLOC1S5-TXNDC5 · 7,884,419C;Ccommon in complete genomicsTypical
- rs1225936BLOC1S5-TXNDC5 · 7,884,951C;Ccommon in complete genomicsTypical
- rs13195786LOC107983965 · 10,163,735A;Acommon on affy axiom dataTypical
- rs12210761LOC107983965 · 10,175,803G;GNo summary available.Typical
- rs11961171NEDD9 · 11,275,795G;Gcommon in complete genomicsTypical
- rs5370EDN1 · 12,296,022G;Tpossibly lower HDL cholesterol in womenMinor
- rs1252951414,096,427T;Tcommon in complete genomicsTypical
- rs7758616LOC105374940 · 14,199,916G;Gcommon genotypeTypical
- rs6914079LOC101928354 · 14,596,134G;Gcommon in complete genomicsTypical
- rs3213207DTNBP1 · 15,627,871T;Tcommon in complete genomicsTypical
- rs2619522DTNBP1 · 15,653,418C;Cassociated with lower attention capacity but also a decrease in positive and paranoid schizotypy scoresWorth knowing
- rs1018381DTNBP1 · 15,656,839A;Aimpaired cognitive abilityWorth knowing
- rs1042391GMPR · 16,290,530T;Tcommon in clinvarTypical
- rs179943ATXN1 · 16,398,087G;Gcommon in complete genomicsTypical
- rs1142345TPMT · 18,130,687C;Cpossibly incapable of detoxifying certain drugsImportant
- rs56161402TPMT · 18,130,762T;TTPMT*8 homozygote; likely issues detoxifying certain drugsWorth knowing
- rs1800584TPMT · 18,130,781T;TTPMT*4A homozygote; likely issues detoxifying certain drugsImportant
- rs2842951TPMT · 18,135,452C;Ccommon in complete genomicsTypical
- rs1800460TPMT · 18,138,997T;Tincapable of detoxifying byproducts of certain drugsImportant
- rs1800462TPMT · 18,143,724G;Gincapable of detoxifying certain drugsImportant
- rs15793179FAS · 18,806,748A;Anormal, for chickensVery important
- rs1688301919,969,407T;Tcommon in complete genomicsTypical
- rs1202199MBOAT1 · 20,155,943C;CNo summary available.Typical
- rs9460521CDKAL1 · 20,567,310G;Gcommon genotypeTypical
- rs10946398CDKAL1 · 20,660,803A;Acommon in clinvarTypical
- rs7754840CDKAL1 · 20,661,019C;C1.3x increased risk for type-2 diabetesImportant
- rs7756992CDKAL1 · 20,679,478A;AnormalTypical
- rs9465871CDKAL1 · 20,717,024C;C2.2x risk type-2 diabetesTypical
- rs6908425CDKAL1 · 20,728,500C;C1.95x increased risk of developing Crohn's diseaseWorth knowing
- rs4712653LINC00340 · 22,125,735C;CSlightly (~1.6x) increased risk for neuroblastomaMinor
- rs9295536LINC00340 · 22,131,700A;A2x increased risk for neuroblastomaTypical
- rs6939340NBAT1 · 22,139,775A;AnormalTypical
- rs423601622,246,375T;Tcommon genotypeTypical
- rs7771911LOC105374975 · 23,437,448C;CNo summary available.Typical
- rs11544636NRSN1 · 24,145,668C;Ccommon in complete genomicsTypical
- rs793862DCDC2 · 24,206,972A;A3-5x dyslexia riskWorth knowing
- rs807701DCDC2 · 24,273,563G;G2-5x increased dyslexia riskWorth knowing
- rs7765678DCDC2 · 24,330,316T;TNo summary available.Typical
- rs2760118ALDH5A1 · 24,503,362C;Ccommon in clinvarTypical
- rs3765310ALDH5A1 · 24,503,369C;Ccommon in complete genomicsTypical
- rs4504469KIAA0319 · 24,588,656C;CcommonTypical
- rs4576240KIAA0319 · 24,596,250G;Gcommon on affy axiom dataTypical
- rs4352670KIAA0319 · 24,603,840A;ANo summary available.Typical
- rs4236032KIAA0319 · 24,606,499A;ANo summary available.Typical
- rs761100KIAA0319 · 24,632,414C;Chigher risk for dyslexiaMinor
- rs2143340TTRAP · 24,658,843G;G> 2x risk of dyslexia and poor reading performanceWorth knowing
- rs17419851LOC105374978 · 24,749,185C;Ccommon on affy axiom dataTypical
- rs2274089LRRC16A · 25,488,355C;Ccommon on affy axiom dataTypical
- rs17342717SLC17A1 · 25,821,542C;Ccommon on affy axiom dataTypical
- rs140827225,842,723T;Tcommon on affy axiom dataTypical
- rs1165205SLC17A3 · 25,870,314T;T0.85x decreased gout riskMinor
- rs9366637LOC108783645 · 26,088,870C;Ccommon in complete genomicsTypical
- rs1799945LOC108783645 · 26,090,951G;GTwo copies of H63D, likely affected by mild form of hemochromatosisVery important
- rs1800562LOC108783645 · 26,092,913A;ATwo copies of C282Y, likely affected by hemochromatosis which may be serious if male or post-menopausal.Very important
- rs198846HIST1H1T · 26,107,235A;ANo summary available.Important
- rs12206204LOC100506979 · 26,116,754C;Ccommon in complete genomicsTypical
- rs13194984BTN1A1 · 26,500,335G;GNo summary available.Typical
- rs1319449127,069,301C;CNo summary available.Typical
- rs13194053TRNAI20 · 27,176,104T;Tcommon on affy axiom dataTypical
- rs6932590TRNAV27 · 27,281,152C;T1.1x increased risk for schizophreniaMinor
- rs1769396327,742,386A;ANo summary available.Typical
- rs9461446NKAPL · 28,259,855C;Ccommon genotypeTypical
- rs13194504ZBED9 · 28,662,914A;ASlightly lower risk for schizophreniaWorth knowing
- rs4324798TRNAF5 · 28,808,340G;Gcommon on affy axiom dataTypical
- rs3749977LOC105375003 · 29,112,567G;Gcommon (highest ability to smell cut grass)Minor
- rs7761746OR5V1 · 29,355,878G;Gcommon genotypeTypical
- rs3749971OR5V1 · 29,374,998G;GNo summary available.Typical
- rs9257809OR5V1 · 29,388,554A;ANo summary available.Typical
- rs1233478LOC105375009 · 29,510,044T;TNo summary available.Worth knowing
- rs362521OR2H2 · 29,588,982C;CNo summary available.Typical
- rs9258260LOC107987427 · 29,755,384C;Ccommon in complete genomicsTypical
- rs12722477HLA-G · 29,828,599C;CNo summary available.Typical
- rs252380929,881,842G;Gcommon in complete genomicsTypical
- rs2916801HLA-A · 29,942,509C;Ccommon in clinvarTypical
- rs2517725HLA-A · 29,943,549A;Acommon in clinvarTypical
- rs2735111HLA-A · 29,943,761T;Tcommon in clinvarTypical
- rs2571381HLA-A · 29,945,053T;Tcommon in clinvarTypical
- rs3823339HLA-A · 29,945,191C;Ccommon in clinvarTypical
- rs3823342HLA-A · 29,945,290T;Tcommon in clinvarTypical
- rs3823343HLA-A · 29,945,334A;Acommon in clinvarTypical
- rs126481329,972,123C;Ccommon/normalTypical
- rs495903929,989,292G;G1.6x higher risk for multiple sclerosisMinor
- rs7758512ZNRD1ASP · 30,002,812T;Tcommon in complete genomicsTypical
- rs9261129HCG8 · 30,011,802T;Tcommon in complete genomicsTypical
- rs9261174ZNRD1ASP · 30,029,078T;Tcommon in complete genomicsTypical
- rs3869068ZNRD1ASP · 30,036,275C;Ccommon in complete genomicsTypical
- rs6917603ZNRD1ASP · 30,049,294T;Tcommon in complete genomicsTypical
- rs8321ZNRD1 · 30,064,745A;Acommon on affy axiom dataTypical
- rs2301753RNF39 · 30,071,463G;Gcommon in complete genomicsTypical
- rs2074480RNF39 · 30,073,033T;Tcommon in complete genomicsTypical
- rs2074479RNF39 · 30,073,232A;Acommon in complete genomicsTypical
- rs34704616TRIM31 · 30,112,592G;Gcommon in complete genomicsTypical
- rs2157678TRIM10 · 30,161,172G;Gcommon on affy axiom dataTypical
- rs3130380HCG18 · 30,311,353G;Gcommon on affy axiom dataTypical
- rs3094628HCG18 · 30,317,535G;Gcommon on affy axiom dataTypical
- rs3130352UBQLN1P · 30,360,580C;Ccommon on affy axiom dataTypical
- rs6902544ABCF1 · 30,580,433A;Acommon genotypeTypical
- rs3094093MDC1-AS1 · 30,711,851A;ANo summary available.Typical
- rs3130660FLOT1 · 30,738,584T;Tcommon on affy axiom dataTypical
- rs10947089LOC105379695 · 30,742,358A;Acommon in complete genomicsTypical
- rs3130783LOC107987453 · 30,806,580G;Gcommon in clinvarTypical
- rs886424LINC00243 · 30,814,225C;Ccommon on affy axiom dataTypical
- rs7772131LINC00243 · 30,827,394A;Acommon genotypeTypical
- rs289405430,904,497G;Gcommon in complete genomicsTypical
- rs2074511VARS2 · 30,921,612T;Tcommon in clinvarTypical
- rs4678VARS2 · 30,926,164G;Gcommon in clinvarTypical
- rs9391637DPCR1 · 30,945,130G;Gcommon genotypeTypical
- rs284468230,978,371A;ANo summary available.Important
- rs4248154MUC22 · 31,034,839C;Ccommon in complete genomicsTypical
- rs284466531,039,078C;Ccommon in complete genomicsTypical
- rs9262632HCG22 · 31,057,031A;Acommon in complete genomicsTypical
- rs494729631,090,401C;CIncreased (2.5x) risk for Graves' diseaseWorth knowing
- rs313054431,090,563C;CNo summary available.Typical
- rs4959053PSORS1C1 · 31,131,800A;AIncreased (>4.4x?) risk of Behcet's diseaseImportant
- rs9263726PSORS1C1 · 31,138,722A;AIn Japanese populations, associated with HLA-B*5801 allele and allopurinol side effectsImportant
- rs9263739CCHCR1 · 31,143,579C;CNo summary available.Typical
- rs746647CCHCR1 · 31,146,405A;Acommon in clinvarTypical
- rs130067CCHCR1 · 31,150,734T;Tcommon in complete genomicsTypical
- rs2073724TCF19 · 31,161,930C;THigher (1.9x) risk for COVID-19 illness being severeMinor
- rs3130501POU5F1 · 31,168,676G;Gcommon in complete genomicsTypical
- rs1265159POU5F1 · 31,172,270A;A22.6x increased psoriasis risk for ChineseWorth knowing
- rs887466PSORS1C3 · 31,175,734T;TNo summary available.Typical
- rs126518131,188,008C;Cpossibly increased risk of psoriasisWorth knowing
- rs6903896HCG27 · 31,200,252G;Gcommon in complete genomicsTypical
- rs18538668031,207,153A;Gcarrier of one HLA-B*38:02:01 allele; avoid thioamide drugsWorth knowing
- rs1049853HLA-C · 31,269,123G;Gcommon in clinvarTypical
- rs2001181HLA-C · 31,269,221C;Ccommon in clinvarTypical
- rs9264594HLA-C · 31,269,271A;Acommon in clinvarTypical
- rs9264601HLA-C · 31,269,577G;Gcommon in clinvarTypical
- rs9264603HLA-C · 31,269,661G;Gcommon in clinvarTypical
- rs9264606HLA-C · 31,269,815A;Acommon in clinvarTypical
- rs9264608HLA-C · 31,269,883A;Acommon in clinvarTypical
- rs707908HLA-C · 31,270,276G;Gcommon in clinvarTypical
- rs9264636HLA-C · 31,270,520C;Ccommon in clinvarTypical
- rs9264638HLA-C · 31,270,541G;Gcommon in clinvarTypical
- rs9264645HLA-C · 31,270,747G;Gcommon in clinvarTypical
- rs9264647HLA-C · 31,270,836A;Acommon in clinvarTypical
- rs9264648HLA-C · 31,270,884G;Gcommon in clinvarTypical
- rs9264664HLA-C · 31,271,450C;Ccommon in clinvarTypical
- rs7383157HLA-C · 31,271,529T;Tcommon in clinvarTypical
- rs9264942LOC107984146 · 31,306,603C;C90% reduction in HIV viral loadWorth knowing
- rs10484554LOC107984146 · 31,306,778C;T2.8x increased risk for psoriasisWorth knowing
- rs313479231,344,549T;Tcommon on affy axiom dataTypical
- rs3819299HLA-B · 31,354,590G;Tlikely to carry one HLA-B27 allele, possible risk for B27 Syndromes.Important
- rs3819294HLA-B · 31,354,710G;Gcommon in clinvarTypical
- rs2523608HLA-B · 31,354,782G;Gcommon in clinvarTypical
- rs3819284MIR6891 · 31,354,990G;Gcommon in clinvarTypical
- rs2523605MIR6891 · 31,355,632T;Tcommon in clinvarTypical
- rs2394985MIR6891 · 31,355,780C;Ccommon in clinvarTypical
- rs2596494MIR6891 · 31,356,061C;Ccommon in clinvarTypical
- rs937824931,359,924T;Tcommon in complete genomicsTypical
- rs7955627931,362,069G;Tincreased risk of Behçet's diseaseVery important
- rs7743761DHFRP2 · 31,368,323A;A20x increased risk of Ankylosing Spondylitis.Worth knowing
- rs9266406DHFRP2 · 31,368,641A;ASlightly increased (>2.3x) risk for Behcet's diseaseWorth knowing
- rs284455931,372,298C;Ccommon on affy axiom dataTypical
- rs13202464FGFR3P1 · 31,376,806A;Glikely to be a carrier of one HLA-B27 allele, possible risk for B27 Syndromes.Important
- rs7654635531,381,371A;Aincreased risk of Behçet's diseaseVery important
- rs12524487LOC105379656 · 31,386,461C;Ccommon genotypeTypical
- rs4349859MICA · 31,398,010A;Alikely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.Important
- rs3763288MICA · 31,402,590G;Gcommon in complete genomicsTypical
- rs1063635MICA · 31,412,154G;Gcommon in clinvarTypical
- rs4418214MICA · 31,423,624T;Tcommon in complete genomicsTypical
- rs2524276LINC01149 · 31,440,488C;CNo summary available.Typical
- rs2255221HCP5 · 31,463,914G;Gcommon in complete genomicsTypical
- rs2395029HCP5 · 31,464,003G;GHLA-B*5701 homozygote likely if Caucasian or Hispanic; high risk for hypersensitivity to various drugs including abacavir; 2x psoriasis risk; see detailsVery important
- rs2230365LOC100287329 · 31,557,671C;Ccommon in complete genomicsTypical
- rs3130062LOC100287329 · 31,558,135T;Tcommon on affy axiom dataTypical
- rs7762619LOC100287329 · 31,563,533T;Tcommon in complete genomicsTypical
- rs2857708LOC100287329 · 31,565,829C;Ccommon in complete genomicsTypical
- rs1041981LOC100287329 · 31,573,007A;AHigher myocardial infarction riskWorth knowing
- rs1800630LOC100287329 · 31,574,699A;A1.8x increased lupus riskTypical
- rs1799724LOC100287329 · 31,574,705C;Tif ApoE4(-), 1.6x risk of AD; if (+), 6.6x riskWorth knowing
- rs1800750TNF · 31,575,186A;Ahigher acute otitis riskTypical
- rs1800629TNF · 31,575,254A;Acomplex; generally higher risk for certain diseasesWorth knowing
- rs361525TNF · 31,575,324A;Acomplex; generally higher risk for certain diseasesTypical
- rs3093662TNF · 31,576,412A;Acommon in complete genomicsTypical
- rs4645843TNF · 31,576,785C;Ccommon genotypeTypical
- rs3093664TNF · 31,576,865A;Acommon in complete genomicsTypical
- rs3093665TNF · 31,577,614A;Acommon in complete genomicsTypical
- rs3093668TNF · 31,578,718G;Gcommon in complete genomicsTypical
- rs3093726TNF · 31,579,012C;CProbably an HLA-B*5701 homozygote; high risk for hypersensitivity to various drugs including abacavirVery important
- rs769177LTB · 31,579,834C;CNo summary available.Typical
- rs986475NCR3 · 31,588,932A;Acommon in complete genomicsTypical
- rs11575839NCR3 · 31,590,014G;GNo summary available.Typical
- rs934887631,607,499C;CNo summary available.Typical
- rs2269475AIF1 · 31,616,154T;Tincreased rheumatoid arthritis riskMinor
- rs2736158MIR6832 · 31,632,527G;Gcommon genotypeTypical
- rs1046089PRRC2A · 31,635,190A;AnormalTypical
- rs3132453BAT2 · 31,636,267G;Gcommon on affy axiom dataTypical
- rs3117582APOM · 31,652,743G;Gincreased lung cancer riskWorth knowing
- rs805264APOM · 31,656,096G;Gcommon in complete genomicsTypical
- rs34490746APOM · 31,657,231T;Tcommon in complete genomicsTypical
- rs707921BAG6 · 31,657,764C;Ccommon genotypeTypical
- rs2075789MSH5-SAPCD1 · 31,740,551C;Ccommon in clinvarTypical
- rs28381349MSH5-SAPCD1 · 31,741,268C;Ccommon in complete genomicsTypical
- rs3131379MSH5 · 31,753,256G;Gcommon on affy axiom dataTypical
- rs1802127MSH5-SAPCD1 · 31,762,148C;Ccommon in complete genomicsTypical
- rs2227956HSPA1L · 31,810,495A;ANo summary available.Typical
- rs9368699C6orf48 · 31,834,764T;Tcommon in complete genomicsTypical
- rs4947332SLC44A4 · 31,866,420C;Ccommon genotypeTypical
- rs11966200SLC44A4 · 31,869,289C;Ccommon on affy axiom dataTypical
- rs497309C2 · 31,924,707A;Acommon on affy axiom dataTypical
- rs9332739C2-AS1 · 31,936,027C;C0.47x decreased risk for AMDWorth knowing
- rs9380272C2-AS1 · 31,938,233G;Gcommon in complete genomicsTypical
- rs547154C2-AS1 · 31,943,161T;T0.47x decreased risk for AMDWorth knowing
- rs4151667CFB · 31,946,247A;Aage related macular degenerationImportant
- rs12614CFB · 31,946,402C;Ccommon in clinvarTypical
- rs641153CFB · 31,946,403G;Gcommon in clinvarTypical
- rs1048709CFB · 31,947,158A;Acommon in clinvarTypical
- rs541862CFB · 31,949,174T;Tcommon on affy axiom dataTypical
- rs4151659CFB · 31,950,687A;Acommon in complete genomicsTypical
- rs1270942CFB · 31,951,083A;Acommon on affy axiom dataTypical
- rs522162CFB · 31,952,140T;Tcommon in complete genomicsTypical
- rs3880457CFB · 31,952,442T;Tcommon in complete genomicsTypical
- rs419788NELFE · 31,961,022T;T2.3x risk for lupusMinor
- rs2734331SKIV2L · 31,962,574A;Acommon in clinvarTypical
- rs429608SKIV2L · 31,962,685G;Gcommon in complete genomicsTypical
- rs2075702DXO · 31,969,734T;Tcommon in complete genomicsTypical
- rs389884DXO · 31,973,120A;ANo summary available.Typical
- rs6467CYP21A2 · 32,039,081C;GCarrier of allele for congenital adrenal hyperplasiaImportant
- rs6474CYP21A2 · 32,039,109G;Gcommon in clinvarTypical
- rs12530380CYP21A2 · 32,039,810A;AMiscall likely if from 23andMe user dataImportant
- rs6476CYP21A2 · 32,039,816A;ACongenital adrenal hyperplasiaVery important
- rs6472CYP21A2 · 32,040,072C;Cbenign polymorphismTypical
- rs7755898CYP21A2 · 32,040,421T;TCongenital adrenal hyperplasiaVery important
- rs12198173TNXB · 32,059,031G;GNo summary available.Typical
- rs185819TNXB · 32,082,290T;Tcommon in clinvarTypical
- rs1150754TNXB · 32,082,981C;Ccommon on affy axiom dataTypical
- rs1720798632,111,790T;Tcommon in complete genomicsTypical
- rs313034232,112,369C;Ccommon on affy axiom dataTypical
- rs204890ATF6B · 32,117,821C;Ccommon in complete genomicsTypical
- rs10947233PPT2 · 32,156,647G;GNo summary available.Typical
- rs17493811AGPAT1 · 32,177,622C;Ccommon in complete genomicsTypical
- rs2071288AGER · 32,181,483C;Ccommon genotypeTypical
- rs2070600AGER · 32,183,666T;T2x higher retinopathy risk in diabetics; 1.5x increased overall risk for gastric cancerWorth knowing
- rs2071292PBX2 · 32,188,171A;Acommon genotypeTypical
- rs3131296NOTCH4 · 32,205,216C;C1.4x increased risk for schizophreniaMinor
- rs2071282NOTCH4 · 32,221,166G;GNo summary available.Typical
- rs3132946NOTCH4 · 32,222,251G;GNo summary available.Typical
- rs54918232,237,268G;Gcommon genotypeTypical
- rs3130340LOC101929163 · 32,276,850T;TNo summary available.Typical
- rs7775397LOC105379657 · 32,293,475T;Tcommon on affy axiom dataTypical
- rs6910071C6orf10 · 32,315,077G;G6x higher risk of rheumatoid arthritisWorth knowing
- rs498422LOC101929163 · 32,318,984G;G>1.42x slightly higher risk for infertility in Chinese menMinor
- rs9469099LOC101929163 · 32,341,131G;Gcommon genotypeTypical
- rs2395148LOC101929163 · 32,353,777G;Gcommon in complete genomicsTypical
- rs3129934LOC101929163 · 32,368,410T;T3.3x increased risk for multiple sclerosisWorth knowing
- rs7758128LOC101929163 · 32,377,506C;Ccommon in complete genomicsTypical
- rs3117103LOC101929163 · 32,381,780A;Acommon on affy axiom dataTypical
- rs1980493LOC101929163 · 32,395,438T;Tcommon on affy axiom dataTypical
- rs2076530LOC101929163 · 32,396,039T;T2x risk for sarcoidosisTypical
- rs3817964LOC101929163 · 32,400,220T;TnormalTypical
- rs3763305LOC101929163 · 32,401,711G;Gcommon in complete genomicsTypical
- rs10947262LOC101929163 · 32,405,535C;C1.3x increased risk for osteoarthritisMinor
- rs940509832,411,959G;Gcommon genotypeTypical
- rs3129878HLA-DRA · 32,440,958C;C>1.36 higher risk for infertility in Chinese menMinor
- rs3135391HLA-DRA · 32,443,210A;A3 to 6 fold higher risk for multiple sclerosisImportant
- rs7192HLA-DRA · 32,443,869T;T3x higher risk for developing a peanut allergyImportant
- rs3135388HLA-DRA · 32,445,274A;A3-6x higher risk of multiple sclerosisWorth knowing
- rs239518532,465,390T;T9.49x risk of Type 1 Diabetes, but 0.58x lower risk of Ulcerative Colitis.Important
- rs66089532,609,603G;G6x higher risk of rheumatoid arthritisWorth knowing
- rs927158832,623,176C;C0.57x risk for Sjogren's syndromeTypical
- rs2842166632,624,960A;Acommon in complete genomicsTypical
- rs4639334LOC107987459 · 32,634,437A;AHomozygous for HLA-DQ7 haplotypeMinor
- rs204041032,634,921C;Ccommon/normalTypical
- rs9272346HLA-DQA1 · 32,636,595A;A18.5x risk for type-1 diabetesImportant
- rs2187668HLA-DQA1 · 32,638,107T;TAutoimmune disorder risk (lupus, celiac disease) due to 2 HLA-DRB1*0301 allelesImportant
- rs17612858HLA-DQA1 · 32,652,845T;Thighest risk (~5x higher) for podoconiosisImportant
- rs9273363HLA-DQB1-AS1 · 32,658,495C;CMuch lower 0.15x risk of Type 1 Diabetes.Worth knowing
- rs2854275HLA-DQB1-AS1 · 32,660,651C;Ccommon in clinvarTypical
- rs777443432,689,801C;CIncreased risk of developing primary biliary cirrhosisWorth knowing
- rs7775228HLA-DQB1 · 32,690,302T;TNo summary available.Typical
- rs946922032,690,533A;A1.5x risk of Crohn's diseaseTypical
- rs471358632,691,805A;Acommon in complete genomicsTypical
- rs645761732,696,074T;T5.2x risk of rheumatoid arthritisWorth knowing
- rs264701232,696,681T;Tslightly increased risk of non-Hodgkin lymphoma in ChineseTypical
- rs264704432,700,133G;Gcommon on affy axiom dataTypical
- rs1175264332,701,596C;Ccommon in complete genomicsTypical
- rs1794265MTCO3P1 · 32,706,960C;CNo summary available.Typical
- rs1252522032,707,693G;Gcommon genotypeTypical
- rs776537932,713,151G;G>1.95x increased risk of Crohn's disease in JapaneseTypical
- rs745410832,713,706C;CHomozygous for HLA-DQ8 haplotypeMinor
- rs9275596LOC100507686 · 32,713,854C;C3x increased risk for developing a peanut allergy, 0.54x risk of IgA Nephropathy in ChineseImportant
- rs3916765LOC102725019 · 32,717,773G;Gcommon on affy axiom dataTypical
- rs285888132,736,068T;Tcommon in complete genomicsTypical
- rs7453920HLA-DOB · 32,762,235G;GSlight increase in risk for chronic hepatitis B infectionMinor
- rs2071554HLA-DOB · 32,816,899C;Ccommon genotypeTypical
- rs241448TAP2 · 32,828,908G;G2.14x increased risk for Alzheimer'sWorth knowing
- rs241447TAP2 · 32,828,974T;Tcommon in clinvarTypical
- rs4148876TAP2 · 32,829,016G;Gcommon genotypeTypical
- rs1800454TAP2 · 32,832,635T;TaffectedMinor
- rs241428TAP2 · 32,836,293T;TNo summary available.Typical
- rs9357155PSMB8 · 32,842,071G;Gcommon on affy axiom dataTypical
- rs1135216TAP1 · 32,847,198T;Tcommon in complete genomicsTypical
- rs1057141TAP1 · 32,850,997T;Tcommon in clinvarTypical
- rs3128935HLA-DOA · 33,004,627T;Tcommon genotypeTypical
- rs43237533,011,902G;Gcommon in complete genomicsTypical
- rs41943433,018,972G;Gcommon in complete genomicsTypical
- rs239530933,058,469A;Acommon in complete genomicsTypical
- rs3077HLA-DPA1 · 33,065,245G;G1.8 times higher odds of having chronic hepatitis BWorth knowing
- rs987870HLA-DPA1 · 33,075,103A;Acommon in complete genomicsTypical
- rs2281388HLA-DPA2 · 33,092,341G;Gcommon in complete genomicsTypical
- rs7763822HLA-DPA2 · 33,092,651C;Ccommon in complete genomicsTypical
- rs7764491HLA-DPA2 · 33,093,063C;Ccommon in complete genomicsTypical
- rs3117242COL11A2P · 33,102,116A;Acommon/normalTypical
- rs3128930COL11A2P · 33,107,889C;Ccommon in complete genomicsTypical
- rs2076310HLA-DPB2 · 33,198,257A;Acommon in complete genomicsTypical
- rs43912133,225,090A;Acommon in complete genomicsTypical
- rs2071888TAPBP · 33,305,078G;Gcommon in clinvarTypical
- rs6457730LOC107986537 · 33,518,955G;GNo summary available.Typical
- rs9469457LOC107986537 · 33,522,105G;Gcommon genotypeTypical
- rs210135BAK1 · 33,572,915A;Acommon in complete genomicsTypical
- rs210138BAK1 · 33,574,761G;GTesticular CancerWorth knowing
- rs561276BAK1 · 33,575,339C;CNo summary available.Typical
- rs3748079ITPR3 · 33,620,370C;C1.9x increased risk for SLE (lupus)Typical
- rs2296336ITPR3 · 33,668,883G;G2.9x risk of type-1 diabetesTypical
- rs2229634ITPR3 · 33,670,403C;Ccommon in complete genomicsTypical
- rs2274459LEMD2 · 33,794,465G;Gcommon on affy axiom dataTypical
- rs774236934,197,944A;Acommon in complete genomicsTypical
- rs177689734,227,234T;Tcommon in complete genomicsTypical
- rs1150781C6orf1 · 34,246,545G;Gcommon in complete genomicsTypical
- rs691898134,270,737A;Acommon in complete genomicsTypical
- rs206936NUDT3 · 34,335,092A;Acommon in complete genomicsTypical
- rs7744392PPARD · 35,354,986A;ANo summary available.Typical
- rs9470004PPARD · 35,374,073C;Ccommon in complete genomicsTypical
- rs7770619PPARD · 35,382,265C;Ccommon genotypeTypical
- rs3798343PPARD · 35,389,916C;Ccommon genotypeTypical
- rs9658108PPARD · 35,395,980C;Ccommon in complete genomicsTypical
- rs2267668PPARD · 35,410,145A;ANo summary available.Typical
- rs2016520PPARD · 35,411,001T;TNo summary available.Typical
- rs645782135,435,028C;CNo summary available.Typical
- rs2064318TULP1 · 35,509,248C;Ccommon in clinvarTypical
- rs7757037FKBP5 · 35,580,459A;A0.63x decreased risk for bipolar disorderTypical
- rs1360780FKBP5 · 35,639,794T;T1.3x increased risk for depressionWorth knowing
- rs4713902FKBP5 · 35,646,249C;C0.47x decreased risk for bipolar disorderTypical
- rs3748051CLPS · 35,797,166T;Tcommon in complete genomicsTypical
- rs2766597CLPS · 35,797,266A;Acommon in complete genomicsTypical
- rs3748050CLPS · 35,797,291T;Tcommon in complete genomicsTypical
- rs1801270CDKN1A · 36,684,194A;Aincreased risk for lung cancerTypical
- rs9394492BTBD9 · 38,364,834C;C<0.76x risk for restless legsTypical
- rs4714156BTBD9 · 38,393,336C;C<0.61x risk for restless legsMinor
- rs9296249BTBD9 · 38,398,065C;C<0.62x risk for restless legsTypical
- rs9357271BTBD9 · 38,398,097T;TNormal risk of developing restless legs syndromeMinor
- rs3923809BTBD9 · 38,473,194A;A1.9x risk for developing restless legs syndromeWorth knowing
- rs17851360GLO1 · 38,682,852T;TNo summary available.Typical
- rs4746GLO1 · 38,682,852T;Tcommon in clinvarTypical
- rs10484854GLO1 · 38,696,818C;CNo summary available.Typical
- rs6923761GLP1R · 39,066,296G;Gcommon/normalTypical
- rs20455KIF6 · 39,357,302G;GNo summary available.Typical
- rs9380880KIF6 · 39,561,206G;Gcommon in complete genomicsTypical
- rs7748513LOC105375056 · 41,160,234A;Acommon genotypeTypical
- rs75932628LOC105375056 · 41,161,514T;Trisk of Alzheimer's diseaseImportant
- rs104894002LOC105375056 · 41,161,557A;GAlzheimer's, late-onset, possible/predictedVery important
- rs3747742TREML2 · 41,194,780G;GNo summary available.Worth knowing
- rs9471576NCR2 · 41,336,067G;Gcommon in complete genomicsTypical
- rs835PRPH2 · 42,698,150C;Ccommon in clinvarTypical
- rs434102PRPH2 · 42,698,323T;Tcommon in clinvarTypical
- rs425876PRPH2 · 42,698,407C;Ccommon in clinvarTypical
- rs390659PRPH2 · 42,698,426G;Gcommon in clinvarTypical
- rs7764439PRPH2 · 42,722,017A;Acommon in clinvarTypical
- rs6458307GLTSCR1L · 42,763,377C;C1.4x riskTypical
- rs1129187PEX6 · 42,964,462G;Gcommon in clinvarTypical
- rs83305243,755,598C;Ccommon in complete genomicsTypical
- rs699947VEGFA · 43,768,652A;A1.36x increased risk for thyroid cancer in menTypical
- rs1570360VEGFA · 43,770,093A;A3x riskTypical
- rs3024994VEGFA · 43,775,770C;Ccommon in complete genomicsTypical
- rs3025035VEGFA · 43,783,622C;Ccommon in complete genomicsTypical
- rs3025039VEGFA · 43,784,799C;T2.6x increased risk for ARMD in a Taiwanese populationWorth knowing
- rs2233434NFKBIE · 44,265,183A;Acommon in complete genomicsTypical
- rs7770848LOC101929770 · 44,801,500T;Tcommon genotypeTypical
- rs10456544SUPT3H · 45,213,957T;Tcommon genotypeTypical
- rs7771980RUNX2 · 45,421,552C;Clower bone mineral density in postmenopausal Korean womenMinor
- rs9472817SLC25A27 · 46,673,255C;CCC genotype increases risk of Alzheimer's in epsilon 4s.Worth knowing
- rs76863441PLA2G7 · 46,709,361C;Ccommon in clinvarTypical
- rs1805018PLA2G7 · 46,711,566A;Acommon in complete genomicsTypical
- rs1805017PLA2G7 · 46,716,485C;Ccommon in clinvarTypical
- rs2103868TNFRSF21 · 47,262,879A;Acommon on affy axiom dataTypical
- rs12175488MUT · 49,456,163C;Ccommon in clinvarTypical
- rs16879498RHAG · 49,612,534C;Ccommon in clinvarTypical
- rs692105950,384,423C;Ccommon genotypeTypical
- rs2817419TFAP2B · 50,845,193G;Gcommon in clinvarTypical
- rs2435322PKHD1 · 52,010,452C;Ccommon in complete genomicsTypical
- rs137852946PKHD1 · 52,024,589T;Tpossible polycystic kidney diseaseVery important
- rs28937907PKHD1 · 52,024,819A;Apossible polycystic kidney diseaseVery important
- rs9296669PKHD1 · 52,026,025G;Gcommon in clinvarTypical
- rs9370096PKHD1 · 52,050,158G;Gcommon in clinvarTypical
- rs2275913IL17A · 52,186,235A;A3x increased gastric cancer risk. Increased risk of Acute Graft-Versus-Host Disease after Unrelated Bone Marrow TransplantationTypical
- rs8193037IL17A · 52,186,311G;Gcommon in complete genomicsTypical
- rs8193038IL17A · 52,186,584A;ANo summary available.Typical
- rs763780IL17F · 52,236,941T;Tcommon on affy axiom dataTypical
- rs11465553IL17F · 52,236,960C;Ccommon in clinvarTypical
- rs2397084IL17F · 52,237,046T;Tcommon in clinvarTypical
- rs7771466IL17F · 52,239,311C;Ccommon genotypeTypical
- rs3804505EFHC1 · 52,438,563A;Arare, related to myoclonic epilepsyWorth knowing
- rs6577GSTA2 · 52,750,617T;Tcommon in complete genomicsTypical
- rs2234951GSTA2 · 52,752,940G;Gcommon on affy axiom dataTypical
- rs4986947GSTA4 · 52,984,432G;Gcommon genotypeTypical
- rs48606053,591,884T;Tcommon in complete genomicsTypical
- rs1688529454,400,598T;Tcommon in complete genomicsTypical
- rs3122169HCRTR2 · 55,248,613A;Acommon in complete genomicsTypical
- rs2653349HCRTR2 · 55,277,539G;G2-6x increased risk for cluster headachesMinor
- rs9367630HCRTR2 · 55,283,305G;Gcommon in complete genomicsTypical
- rs11758339DST · 56,463,051C;CNo summary available.Typical
- rs4715630DST · 56,552,484T;TNo summary available.Typical
- rs11756977DST · 56,555,740C;CNo summary available.Typical
- rs10484410ZNF451 · 57,131,890A;ANo summary available.Typical
- rs1040461RAB23 · 57,190,556C;Ccommon in complete genomicsTypical
- rs9352774LGSN · 63,304,907A;Acommon in complete genomicsTypical
- rs11754641EYS · 64,926,030C;Ccommon genotypeTypical
- rs12216299EYS · 65,412,466T;Tcommon in complete genomicsTypical
- rs944573266,538,517G;Gcommon genotypeTypical
- rs6910140COL9A1 · 70,234,554T;Tcommon in clinvarTypical
- rs1196881471,067,268G;Gcommon in complete genomicsTypical
- rs970547COL12A1 · 75,087,586C;Ccommon in clinvarTypical
- rs13212041LOC105377864 · 77,461,407C;CNo summary available.Typical
- rs16889859LOC105377865 · 78,316,148A;Acommon in complete genomicsTypical
- rs1689033478,846,449T;Tcommon genotypeTypical
- rs3747767SH3BGRL2 · 79,547,564C;Ccommon on affy axiom dataTypical
- rs1321847C6orf7 · 79,823,470G;Gcommon genotypeTypical
- rs3812153ELOVL4 · 79,916,658T;Tcommon in clinvarTypical
- rs28934895BCKDHB · 80,168,945C;CMaple syrup urine diseaseVery important
- rs79761867BCKDHB · 80,168,945C;CMaple Syrup Urine diseaseVery important
- rs1321324780,806,319A;Acommon in complete genomicsTypical
- rs6924906LOC105377871 · 81,510,835T;Tcommon genotypeTypical
- rs1689352681,805,598G;Gcommon on affy axiom dataTypical
- rs49456285,407,411A;Acommon in complete genomicsTypical
- rs806606LOC101928842 · 85,974,061C;CNo summary available.Typical
- rs3828741HTR1E · 87,015,956G;Gcommon in complete genomicsTypical
- rs1925690ZNF292 · 87,157,345C;Ccommon on affy axiom dataTypical
- rs13213285ORC3 · 87,620,224C;CNo summary available.Typical
- rs2509458LOC105377882 · 87,942,862T;Tcommon on affy axiom dataTypical
- rs806368CNR1 · 88,140,381C;CAssociated with Alcohol Dependence; associated with nicotine dependence (female)Worth knowing
- rs12720071CNR1 · 88,141,462T;Tcommon in complete genomicsTypical
- rs1049353CNR1 · 88,143,916T;TLikely better response to antidepressants if femaleMinor
- rs806380CNR1 · 88,154,934G;Guncommon. lowest odds of cannabis dependenceWorth knowing
- rs16880441RPS14P9 · 88,266,258C;Ccommon in complete genomicsTypical
- rs10485165LOC105377885 · 88,403,098C;Ccommon on affy axiom dataTypical
- rs1175766188,473,861G;Gcommon genotypeTypical
- rs6939321ANKRD6 · 89,589,491C;Ccommon genotypeTypical
- rs6454764ANKRD6 · 89,601,247C;Ccommon in complete genomicsTypical
- rs16870040LOC105377896 · 92,592,553A;Acommon in complete genomicsTypical
- rs332951LOC105377896 · 92,597,090C;CNo summary available.Typical
- rs250693392,905,732T;Tcommon in complete genomicsTypical
- rs140828293,142,534G;Gcommon on affy axiom dataTypical
- rs2278107EPHA7 · 93,410,921T;Tcommon in complete genomicsTypical
- rs9345389TSG1 · 93,730,886A;Acommon in complete genomicsTypical
- rs430264794,056,539G;Gcommon in complete genomicsTypical
- rs9387522MANEA · 95,607,059A;Aincreased risk of cocaine induced paranoia.Typical
- rs1320832196,412,478A;Aslight increase in risk for migraineMinor
- rs1252987498,014,625G;Gcommon genotypeTypical
- rs949164098,471,388C;Ccommon in complete genomicsTypical
- rs138380898,580,990T;Tcommon genotypeTypical
- rs17185536100,173,055T;Tslight increase in risk for ED in menMinor
- rs2841307100,308,811C;Ccommon in complete genomicsTypical
- rs3734355LOC102724406 · 100,420,845G;Gcommon in clinvarTypical
- rs3734354SIM1 · 100,420,903G;Gcommon in clinvarTypical
- rs3734353SIM1 · 100,448,693T;Tcommon in clinvarTypical
- rs240768ASCC3 · 100,509,468T;Tcommon genotypeTypical
- rs11969893LOC102724422 · 100,947,531G;GNo summary available.Typical
- rs2518224GRIK2 · 101,458,776A;AnormalTypical
- rs4520040103,984,290G;Gcommon in complete genomicsTypical
- rs9377619104,145,992A;Acommon on affy axiom dataTypical
- rs733724HACE1 · 104,775,989G;GNo summary available.Typical
- rs7759938104,931,079C;Cage at menarche ~2 months later on averageTypical
- rs12194974LIN28B · 104,956,323G;Gcommon in complete genomicsTypical
- rs6911490PRDM1 · 106,074,152C;Ccommon on affy axiom dataTypical
- rs9372120ATG5 · 106,219,660T;Tcommon/normalTypical
- rs783396AIM1 · 106,539,495C;Ccommon in complete genomicsTypical
- rs2430457PDSS2 · 107,339,442A;Acommon genotypeTypical
- rs17069122RPL3P7 · 108,002,555G;Gcommon in complete genomicsTypical
- rs2802288FOXO3 · 108,575,012A;Alonger lifespanWorth knowing
- rs2802292FOXO3 · 108,587,315G;G1.5x~2.7x more likely to live to 100.Worth knowing
- rs2764264FOXO3 · 108,613,258C;Cgreater odds of living to 95Worth knowing
- rs12212067FOXO3 · 108,659,993G;GLower inflammatory responseMinor
- rs1935949FOXO3 · 108,678,084A;A1.46 OR for reaching "exceptional longevity"Worth knowing
- rs9400317AKD1 · 109,686,444G;Gcommon on affy axiom dataTypical
- rs121908287FIG4 · 109,715,133C;Chomozygote for I41T partial function variantVery important
- rs4947019FIG4 · 109,768,846C;Ccommon in complete genomicsTypical
- rs3204953REV3L · 111,307,423G;GNo summary available.Typical
- rs458017REV3L · 111,374,888T;Tcommon on affy axiom dataTypical
- rs3851228LOC107986522 · 111,526,988A;Acommon genotypeTypical
- rs13190932TRAF3IP2 · 111,591,867G;Gcommon on affy axiom dataTypical
- rs1230345WISP3 · 112,061,110G;Gcommon in clinvarTypical
- rs17073260WISP3 · 112,061,120C;Ccommon in clinvarTypical
- rs9488238VN1R13P · 113,695,931A;ANo summary available.Typical
- rs11391HDAC2 · 113,940,851A;ANo summary available.Typical
- rs10499080HDAC2 · 113,952,482C;Ccommon in complete genomicsTypical
- rs3812111COL10A1 · 116,122,572T;Tcommon in clinvarTypical
- rs784133RSPH4A · 116,629,670T;Tcommon in clinvarTypical
- rs654128FAM162B · 116,765,215C;Ccommon on affy axiom dataTypical
- rs339331RFX6 · 116,888,889T;TProstate cancer riskWorth knowing
- rs619203ROS1 · 117,301,021C;Gincreases susceptibility to Myocardial Infarction 1.15 timesMinor
- rs529156ROS1 · 117,301,025C;CNo summary available.Typical
- rs529038ROS1 · 117,301,070T;TNo summary available.Typical
- rs2243380ROS1 · 117,403,216G;GNo summary available.Typical
- rs12210810118,332,041G;Gcommon in complete genomicsTypical
- rs25422CEP85L · 118,486,684C;Ccommon in complete genomicsTypical
- rs2817937120,777,311T;Tcommon on affy axiom dataTypical
- rs2789066120,778,991G;Gcommon in complete genomicsTypical
- rs17083533121,409,576G;Gcommon genotypeTypical
- rs2279381FABP7 · 122,780,399T;TMore fragmented sleep (no particular negative consequences)Worth knowing
- rs9490550FABP7 · 122,783,162G;Gcommon/normalTypical
- rs529858NCOA7-AS1 · 125,816,778G;GNo summary available.Typical
- rs972275LOC105377989 · 127,070,699C;CNo summary available.Typical
- rs192408THEMIS · 127,819,318G;Gcommon in complete genomicsTypical
- rs10499138PTPRK · 128,171,037A;Acommon in complete genomicsTypical
- rs1891150PTPRK · 128,442,284A;Acommon genotypeTypical
- rs9492297LAMA2 · 129,291,613G;Gcommon in clinvarTypical
- rs12193446LAMA2 · 129,498,893G;Glower risk of nearsightednessWorth knowing
- rs12205363LAMA2 · 129,513,484T;TNo summary available.Typical
- rs17057678ARHGAP18 · 129,710,348T;TnormalTypical
- rs7769153EPB41L2 · 130,935,224T;Tcommon genotypeTypical
- rs6917207AKAP7 · 131,149,096C;Ccommon in complete genomicsTypical
- rs997509ENPP1 · 131,846,837C;Ccommon in complete genomicsTypical
- rs6917644LOC100131774 · 131,944,525A;Acommon in complete genomicsTypical
- rs9399005CTGF · 131,947,824C;Ccommon in complete genomicsTypical
- rs6918698CTGF · 131,952,117C;Cnormal riskTypical
- rs9402373LOC100131774 · 131,956,291C;Ccommon in complete genomicsTypical
- rs8192625TAAR6 · 132,571,193G;Gcommon on affy axiom dataTypical
- rs9493627EYA4 · 133,468,590G;Gcommon in clinvarTypical
- rs9402515TARID · 133,539,207A;Acommon on affy axiom dataTypical
- rs9402571SGK1 · 134,167,822G;G0.85x decreased risk for type-2 diabetesMinor
- rs1763500LOC107986646 · 134,223,595A;Acommon genotypeTypical
- rs9493873SGK1 · 134,255,373T;Tcommon genotypeTypical
- rs11755699SGK1 · 134,278,109T;Tcommon genotypeTypical
- rs4895441LOC105378010 · 135,105,435A;Acommon in clinvarTypical
- rs117447608AHI1 · 135,318,577A;GPathogenicity unclear; possible carrier of a Joubert syndrome mutationWorth knowing
- rs1535435AHI1 · 135,435,884A;ANo summary available.Typical
- rs9494266C6orf217 · 135,530,435G;GNo summary available.Typical
- rs9389316LINC00271 · 135,679,865C;Ccommon genotypeTypical
- rs11154851LOC644135 · 136,046,867C;Ccommon genotypeTypical
- rs3799488IFNGR1 · 137,198,643T;Tcommon in complete genomicsTypical
- rs1327475IFNGR1 · 137,215,318G;Gcommon on affy axiom dataTypical
- rs7749390IFNGR1 · 137,219,233A;Acommon in clinvarTypical
- rs2234711IFNGR1 · 137,219,383A;Acommon in clinvarTypical
- rs13207033137,644,281A;Areduced risk of rheumatoid arthritisWorth knowing
- rs13192841137,646,077A;Asomewhat reduced risk (~0.5x) for lupusWorth knowing
- rs10499194137,681,500T;Tprotective against rheumatoid arthritis for asiansWorth knowing
- rs6920220137,685,367A;A1.7x risk of Rheumatoid ArthritisImportant
- rs7753394137,764,111C;C1.5x risk of Crohn's diseaseTypical
- rs10499197137,811,379T;Tcommon genotypeTypical
- rs9494883LOC100130476 · 137,850,329A;Acommon in complete genomicsTypical
- rs5029937TNFAIP3 · 137,874,014G;GNo summary available.Typical
- rs5029939TNFAIP3 · 137,874,586C;Ccommon in complete genomicsTypical
- rs2230926TNFAIP3 · 137,874,929G;G1.4x risk of rheumatoid arthritisWorth knowing
- rs582757TNFAIP3 · 137,876,687C;Gcandidate causal variant of psoriasisMinor
- rs7752903137,906,227T;Tcommon genotypeTypical
- rs6932056137,921,300T;TNo summary available.Typical
- rs9321637LOC105378020 · 137,945,548T;Tcommon in complete genomicsTypical
- rs642858139,952,510G;Gcommon in complete genomicsTypical
- rs11155133LOC102723724 · 140,848,688A;Acommon in complete genomicsTypical
- rs6570465141,535,457C;Ccommon genotypeTypical
- rs7742587141,535,997C;Ccommon genotypeTypical
- rs17071124141,712,589A;Acommon genotypeTypical
- rs9496398142,501,080T;Tcommon in complete genomicsTypical
- rs6923492GRM1 · 146,434,188T;Tcommon in clinvarTypical
- rs1302019SAMD5 · 147,650,438T;TNo summary available.Typical
- rs9497975SASH1 · 148,226,666G;Gcommon in complete genomicsTypical
- rs2500535UST · 149,008,131G;Gcommon on affy axiom dataTypical
- rs727979TAB2 · 149,272,784C;Ccommon/normalTypical
- rs9485370TAB2 · 149,285,665G;Gcommon/normalTypical
- rs9485372TAB2 · 149,287,738G;Gcommon in complete genomicsTypical
- rs237025SUMO4 · 149,400,554A;Ano credible riskTypical
- rs1853665LOC100506038 · 149,977,706C;Ccommon in complete genomicsTypical
- rs803424MTHFD1L · 150,885,030C;CNo summary available.Typical
- rs11754661MTHFD1L · 150,885,942G;Gcommon on affy axiom dataTypical
- rs6922269MTHFD1L · 150,931,849A;A1.6x risk of coronary artery diseaseWorth knowing
- rs12525353MTHFD1L · 150,978,896C;Ccommon in complete genomicsTypical
- rs3757318C6orf97 · 151,592,978G;Gcommon in complete genomicsTypical
- rs1038304LOC107986528 · 151,612,040A;GNo summary available.Typical
- rs6929137LOC107986528 · 151,615,542G;Gcommon in clinvarTypical
- rs3734805LOC107986528 · 151,618,215A;Acommon in complete genomicsTypical
- rs12665607LOC105378058 · 151,625,494T;Tcommon in clinvarTypical
- rs2046210151,627,231A;A1.6x increased breast cancer risk in certain womenMinor
- rs9397435151,630,085A;Acommon in complete genomicsTypical
- rs140068132151,633,699A;Glower risk for breast cancerWorth knowing
- rs10484919ESR1 · 151,653,287C;Ccommon in complete genomicsTypical
- rs9383938ESR1 · 151,666,222G;Gcommon in complete genomicsTypical
- rs2881766ESR1 · 151,797,984G;TSlightly increased risk for pregnancy-induced hypertensionMinor
- rs11964281ESR1 · 151,800,307C;CNo summary available.Typical
- rs9340799ESR1 · 151,842,246G;GWomen have 10x risk of Endometriosis, but half the risk of Endometrial Cancer and 0.76x less cognitive impairment.Important
- rs3020314ESR1 · 151,949,537C;C0.42x reduced lymphoma riskTypical
- rs9383951ESR1 · 151,974,478G;Gcommon in complete genomicsTypical
- rs2179922ESR1 · 151,975,965A;Amales 1-2cm shorter on averageTypical
- rs728524ESR1 · 151,982,302A;Acommon in complete genomicsTypical
- rs7757956ESR1 · 151,996,005T;Tcommon in complete genomicsTypical
- rs2228480ESR1 · 152,098,960G;Gcommon in complete genomicsTypical
- rs3798758ESR1 · 152,100,719C;Ccommon in complete genomicsTypical
- rs2295190ESR1 · 152,122,609T;TSlightly increased risk for ovarian cancer in womenMinor
- rs7747960SYNE1 · 152,470,339C;Ccommon in complete genomicsTypical
- rs13218732152,944,075A;Acommon genotypeTypical
- rs73568641153,704,004C;CFor African Americans in treatment, possible methadone dose adjustmentMinor
- rs1799971OPRM1 · 154,039,662G;Gmore painWorth knowing
- rs563649OPRM1 · 154,086,832C;Ccommon in complete genomicsTypical
- rs10485057OPRM1 · 154,092,120G;Gincreased risk for smoking, nicotine dependenceImportant
- rs2281617OPRM1 · 154,166,286C;CNormal (better) response to amphetamineWorth knowing
- rs2275336CNKSR3 · 154,405,854G;Gcommon genotypeTypical
- rs35229355155,608,667C;Ccommon in complete genomicsTypical
- rs2163287ZDHHC14 · 157,620,251G;Gcommon in complete genomicsTypical
- rs4709267TAGAP · 159,035,343A;Acommon in complete genomicsTypical
- rs394581LOC105378083 · 159,061,489C;Chigher risk of RA in African and Hispanic populationsTypical
- rs5746151SOD2 · 159,680,288C;Ccommon genotypeTypical
- rs5746134SOD2 · 159,682,083G;Gcommon in complete genomicsTypical
- rs4880SOD2 · 159,692,840G;Gcomplex! see rs4880Minor
- rs4516970SOD2 · 159,716,655G;Gcommon in complete genomicsTypical
- rs6917747IGF2R · 159,981,673G;Gcommon on affy axiom dataTypical
- rs8191754IGF2R · 160,027,292C;Ccommon in complete genomicsTypical
- rs2282143SLC22A1 · 160,136,611C;Ccommon on affy axiom dataTypical
- rs622342SLC22A1 · 160,151,834C;Cinfluences dosage for Parkinson's patientsWorth knowing
- rs8177517SLC22A2 · 160,242,388T;Tcommon in complete genomicsTypical
- rs8177516SLC22A2 · 160,243,653G;Gcommon in complete genomicsTypical
- rs316019SLC22A2 · 160,249,250C;Ccommon in complete genomicsTypical
- rs12214416LPAL2 · 160,489,485T;Tcommon in complete genomicsTypical
- rs3798220LPA · 160,540,105C;C2-3x higher risk for cardiovascular events, which can be lowered by aspirinWorth knowing
- rs10455872LPA · 160,589,086G;G2,57x increased Coronary Heart disease riskImportant
- rs9457951LPA · 160,606,796C;Ccommon in complete genomicsTypical
- rs2314378MAP3K4 · 161,059,100A;Acommon in complete genomicsTypical
- rs1801334PARK2 · 161,360,193C;Ccommon in clinvarTypical
- rs992037PARK2 · 161,580,404C;Clowest lysine valuesTypical
- rs3016539PARK2 · 161,815,043T;Tcommon in complete genomicsTypical
- rs391695LOC100289273 · 164,104,554G;Gcommon in complete genomicsTypical
- rs3008052PDE10A · 165,653,494C;Ccommon/normalTypical
- rs1039002PDE10A · 165,741,969G;Gcommon in complete genomicsTypical
- rs12195036LOC105378117 · 166,038,209T;Tcommon genotypeTypical
- rs2305089T · 166,165,782T;Thigher risk for chordoma reported in one study; no association seen in another studyMinor
- rs2301436FGFR1OP · 167,024,500T;TNo summary available.Worth knowing
- rs1473500168,110,336C;Ccommon genotypeTypical
- rs13208776SMOC2 · 168,540,944A;AnormalTypical
- rs8089LOC101929523 · 169,217,631C;Cslightly increased heart attack riskTypical
- rs3734905WDR27 · 169,558,886G;Gcommon on affy axiom dataTypical
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.