Chromosome 8
274 well-documented SNPs on chromosome 8, in order of position (GRCh38).
- rs17665859C8orf42 · 495,601T;Tcommon on affy axiom dataTypical
- rs17666538ERICH1 · 616,207T;TNo summary available.Typical
- rs13279485LOC100131395 · 1,935,186T;TNo summary available.Typical
- rs6415252,882,980T;Tcommon in complete genomicsTypical
- rs2623702CSMD1 · 3,737,384T;Tcommon in complete genomicsTypical
- rs1454292RSL24D1P7 · 5,068,943C;Ccurlier hairWorth knowing
- rs17076812MCPH1 · 6,421,917A;Acommon in complete genomicsTypical
- rs2442513MCPH1 · 6,439,029T;Tcommon genotypeTypical
- rs930557MCPH1 · 6,444,662G;Gcommon in clinvarTypical
- rs2515569MCPH1 · 6,444,897G;Gcommon in complete genomicsTypical
- rs1129703MCPH1 · 6,447,173G;Gcommon in complete genomicsTypical
- rs1129706MCPH1 · 6,447,293G;Gcommon in complete genomicsTypical
- rs2034143MCPH1 · 6,453,217G;Gcommon in complete genomicsTypical
- rs2916733MCPH1 · 6,465,757G;Gcommon in complete genomicsTypical
- rs12674488MCPH1 · 6,480,785C;Ccommon in clinvarTypical
- rs17077154MCPH1 · 6,493,731T;Tcommon in complete genomicsTypical
- rs2515475ANGPT2 · 6,530,918C;CnormalTypical
- rs1057090MCPH1-AS1 · 6,621,521C;Ccommon in clinvarTypical
- rs1057091MCPH1-AS1 · 6,643,023C;Ccommon in clinvarTypical
- rs1800971DEFB1 · 6,870,594T;Tcommon in complete genomicsTypical
- rs1047031DEFB1 · 6,870,676T;T1.3x increased risk for periodontitisMinor
- rs11362DEFB1 · 6,877,877C;TNo summary available.Minor
- rs1800972DEFB1 · 6,877,901C;Creduced risk for Crohn's disease; reduced risk for maternal HIV transmissionWorth knowing
- rs27381736,883,416A;Acommon in complete genomicsTypical
- rs27381696,885,036A;ANo summary available.Typical
- rs10108954MFHAS1 · 8,864,868C;Ccommon in complete genomicsTypical
- rs1897989,133,067A;Adecreased high myopia riskWorth knowing
- rs3748140PPP1R3B · 9,141,509C;Ccommon on affy axiom dataTypical
- rs9987289LOC157273 · 9,325,848G;Gcommon on affy axiom dataTypical
- rs6601299LOC157273 · 9,327,181C;CNo summary available.Typical
- rs2126259LOC157273 · 9,327,636C;CNo summary available.Typical
- rs273634011,486,464T;TNo summary available.Worth knowing
- rs1327711311,491,677A;ANo summary available.Worth knowing
- rs2255327BLK · 11,552,483C;CNo summary available.Typical
- rs804280GATA4 · 11,755,189C;Ccommon in clinvarTypical
- rs3729856GATA4 · 11,757,066A;Acommon in clinvarTypical
- rs6601606NEIL2 · 11,780,735A;Acommon on affy axiom dataTypical
- rs12720208FGF20 · 16,992,890G;Gcommon in clinvarTypical
- rs10090288MICU3 · 17,072,126A;Acommon in complete genomicsTypical
- rs2720508ADAM24P · 17,472,318T;Tcommon in complete genomicsTypical
- rs445422PCM1 · 17,935,584C;CNo summary available.Typical
- rs10103355ASAH1 · 18,061,425A;Acommon in clinvarTypical
- rs1071645ASAH1 · 18,071,302C;Ccommon in clinvarTypical
- rs1712623218,120,141C;Ccommon in complete genomicsTypical
- rs28359483NAT1 · 18,210,188G;Gcommon in complete genomicsTypical
- rs4986988NAT1 · 18,221,704C;Ccommon genotypeTypical
- rs4987076NAT1 · 18,222,492A;GNAT1*17 alleleMinor
- rs4986782NAT1 · 18,222,607A;Aslow acetylator = higher risk of smoking-induced lung cancerImportant
- rs15561NAT1 · 18,223,142C;CNo summary available.Typical
- rs1801279NAT2 · 18,400,194G;Gcommon in complete genomicsTypical
- rs1041983NAT2 · 18,400,285C;Ccommon in clinvarTypical
- rs1801280NAT2 · 18,400,344T;Tcommon in clinvarTypical
- rs4986996NAT2 · 18,400,367G;Gcommon in complete genomicsTypical
- rs4986997NAT2 · 18,400,414A;Acommon in complete genomicsTypical
- rs1799929NAT2 · 18,400,484C;CNo summary available.Typical
- rs1799930NAT2 · 18,400,593A;ASomewhat increased risk of hearing lossWorth knowing
- rs1208NAT2 · 18,400,806A;ANo summary available.Typical
- rs1799931NAT2 · 18,400,860G;Gcommon in clinvarTypical
- rs492191418,414,928T;Tcommon in complete genomicsTypical
- rs149574118,415,371A;ANAT2 slow metabolizer (predicted)Worth knowing
- rs149574318,415,790C;Ccommon in complete genomicsTypical
- rs1800590LPL · 19,939,160T;Tcommon in complete genomicsTypical
- rs1121923LPL · 19,951,924G;Gcommon in clinvarTypical
- rs268LPL · 19,956,018G;G3X+ increased risk for venous thromboembolismWorth knowing
- rs321LPL · 19,961,675G;Gcommon in complete genomicsTypical
- rs325LPL · 19,961,817T;TNo summary available.Typical
- rs326LPL · 19,961,928A;Alower HDL cholesterolWorth knowing
- rs328LPL · 19,962,213C;Ccommon in clinvarTypical
- rs4922115LPL · 19,965,319G;Gcommon in clinvarTypical
- rs1059611LPL · 19,967,052T;Tcommon in clinvarTypical
- rs15285LPL · 19,967,156C;Ccommon in clinvarTypical
- rs1748275319,975,135G;GnormalTypical
- rs1267891919,986,711A;Gassociated with higher HDL cholesterolWorth knowing
- rs1050366919,990,179A;Aassociated with higher HDL cholesterolWorth knowing
- rs208363720,007,664A;ANo summary available.Typical
- rs701688020,019,235G;Gcommon on affy axiom dataTypical
- rs2270641SLC18A1 · 20,180,955G;G3.7x higher risk for schizophreniaWorth knowing
- rs723874LZTS1 · 20,250,090G;Gcommon in complete genomicsTypical
- rs7014851HR · 22,119,197C;CNo summary available.Typical
- rs4715SFTPC · 22,163,524C;Ccommon in clinvarTypical
- rs4871976PHYHIP · 22,228,978A;Acommon in complete genomicsTypical
- rs4872511SORBS3 · 22,543,476C;Ccommon in complete genomicsTypical
- rs1047266TNFRSF10B · 23,043,188G;Gcommon on affy axiom dataTypical
- rs13278062TNFRSF10A · 23,225,458G;Gcommon in clinvarTypical
- rs2979704NEFL · 24,951,554C;Ccommon in clinvarTypical
- rs1059111NEFL · 24,952,575T;Tcommon in clinvarTypical
- rs751141EPHX2 · 27,516,348G;Gcommon in clinvarTypical
- rs17057381EPHX2 · 27,559,284G;Gcommon genotypeTypical
- rs11136000CLU · 27,607,002C;T0.84x decreased risk for Alzheimer's diseaseMinor
- rs11779594PNOC · 28,324,238C;CNo summary available.Typical
- rs10096097DCTN6 · 30,169,582G;Gincreased Anorexia Nervosa riskWorth knowing
- rs2230009WRN · 31,064,419G;Gcommon in clinvarTypical
- rs3087425WRN · 31,120,294C;Ccommon in clinvarTypical
- rs1801195WRN · 31,141,764G;Gcommon in clinvarTypical
- rs11574358WRN · 31,147,066T;Tcommon genotypeTypical
- rs3575350531,616,625C;CNo summary available.Worth knowing
- rs6994992NRG1 · 31,638,065C;TNo summary available.Minor
- rs10503887NRG1 · 31,775,931G;Gcommon on affy axiom dataTypical
- rs6996585NRG1 · 32,543,285A;Acommon/normalTypical
- rs16879552NRG1 · 32,553,698C;Ccommon in complete genomicsTypical
- rs3924999NRG1 · 32,595,840C;TNo summary available.Typical
- rs10503929NRG1 · 32,756,465T;TNo summary available.Typical
- rs699025534,269,430C;Ccommon in complete genomicsTypical
- rs260965334,379,474A;ANo summary available.Typical
- rs7816345RPL26P25 · 36,988,591C;Cbigger breast size (normal in European)Worth knowing
- rs6468442ADGRA2 · 37,829,231G;Gcommon on affy axiom dataTypical
- rs4994ADRB3 · 37,966,280G;G2x higher risk in certain women for cardiac events; associated with elite endurance performance in menWorth knowing
- rs104894086STAR · 38,146,068T;TLipoid congenital adrenal hyperplasia (LCAH); treatment requiredVery important
- rs16887217STAR · 38,146,907T;Tcommon/normalTypical
- rs193922393STAR · 38,148,684-;-Lipoid congenital adrenal hyperplasia (LCAH); treatment requiredVery important
- rs13317FGFR1 · 38,411,996T;Tcommon in clinvarTypical
- rs515071ANK1 · 41,661,944A;Acommon in clinvarTypical
- rs4737009ANK1 · 41,772,887G;Gcommon in complete genomicsTypical
- rs2020921PLAT · 42,187,447G;Gcommon genotypeTypical
- rs12676482IKBKB · 42,316,559G;Gcommon genotypeTypical
- rs4950CHRNB3 · 42,697,490A;AMost common genotype in several populations; yet also higher leadership occupancy?Minor
- rs4953CHRNB3 · 42,732,516G;Gcommon in complete genomicsTypical
- rs7003908PRKDC · 47,858,141A;AnormalTypical
- rs8178085PRKDC · 47,898,144T;Tcommon in complete genomicsTypical
- rs1177832948,140,605C;Ccommon on affy axiom dataTypical
- rs10504130PCMTD1 · 51,844,533G;Gcommon/normalTypical
- rs1095840954,414,531A;A1.79x increased aneurysm riskTypical
- rs9298506RP1 · 54,524,964A;A~1.46x increased risk of aneurysmTypical
- rs444772RP1 · 54,626,497G;Gcommon in clinvarTypical
- rs2293869RP1 · 54,626,835A;Acommon in clinvarTypical
- rs446227RP1 · 54,628,890G;Gcommon in clinvarTypical
- rs414352RP1 · 54,628,953T;Tcommon in clinvarTypical
- rs12542677XKR4 · 55,255,499C;CNo summary available.Typical
- rs10504249LOC105375856 · 57,876,522A;Acommon genotypeTypical
- rs11994937NSMAF · 58,596,021C;CNo summary available.Typical
- rs11780640NSMAF · 58,603,001T;Tcommon in complete genomicsTypical
- rs96008958,795,750C;Ccommon in complete genomicsTypical
- rs6995588LOC105375861 · 60,091,338C;Ccommon in complete genomicsTypical
- rs903027CLVS1 · 61,496,869T;Tcommon in complete genomicsTypical
- rs1031552GGH · 63,020,631G;Gcommon in complete genomicsTypical
- rs11545078GGH · 63,026,205G;Gcommon on affy axiom dataTypical
- rs3824333GGH · 63,028,658T;Tcommon in complete genomicsTypical
- rs4617146GGH · 63,030,158C;Ccommon in complete genomicsTypical
- rs10504390MTFR1 · 65,711,997A;ANo summary available.Typical
- rs460129265,939,496G;Gcommon in complete genomicsTypical
- rs13279522DNAJC5B · 66,062,017T;Tcommon in complete genomicsTypical
- rs12721510CRH · 66,178,947T;TRisk for ACTH deficiencyTypical
- rs699091767,887,142T;Tcommon in complete genomicsTypical
- rs1517114C8orf34 · 68,476,982C;Ccommon in clinvarTypical
- rs16935279LINC01592 · 68,961,217T;Tcommon genotypeTypical
- rs16936455SLCO5A1 · 69,812,519A;Acommon on affy axiom dataTypical
- rs1199403472,158,500C;Ccommon genotypeTypical
- rs16938910GDAP1 · 74,461,713C;Ccommon in complete genomicsTypical
- rs10106137MIR2052HG · 74,615,398C;CNo summary available.Typical
- rs16939046CASC9 · 75,235,719T;Tcommon on affy axiom dataTypical
- rs10087163PEX2 · 76,983,629A;Acommon in clinvarTypical
- rs386466377,768,114T;Tcommon in complete genomicsTypical
- rs1520333LOC105375911 · 78,488,803G;GNo summary available.Typical
- rs146016379,315,213G;Gcommon in complete genomicsTypical
- rs1198767880,316,591T;Tcommon genotypeTypical
- rs11782652CHMP4C · 81,741,409A;ANo summary available.Typical
- rs13264970LOC105375929 · 82,161,594C;Tcommon in complete genomicsTypical
- rs701562282,991,579A;Acommon in complete genomicsTypical
- rs7827474CA1 · 85,329,459G;Gcommon in complete genomicsTypical
- rs2228063CA2 · 85,480,760A;AcommonTypical
- rs3735972CNGB3 · 86,575,970C;CNo summary available.Minor
- rs13265557CNGB3 · 86,647,872C;Crare variation in a gene influencing color perceptionTypical
- rs4961206CNGB3 · 86,654,023T;Tcommon in clinvarTypical
- rs6471482CNGB3 · 86,667,075A;ANo summary available.Minor
- rs1050486188,535,703T;TReduced risk of migraine without auraWorth knowing
- rs439744989,329,957G;Gcommon in complete genomicsTypical
- rs1063054NBN · 89,934,373T;Tcommon in clinvarTypical
- rs2735383NBN · 89,935,041C;Ccommon in clinvarTypical
- rs1061302NBN · 89,946,194T;Tcommon in clinvarTypical
- rs709816NBN · 89,955,483A;Acommon in clinvarTypical
- rs587776650NBN · 89,971,214-;-Nijmegen breakage syndromeVery important
- rs769416NBN · 89,971,229G;Gcommon in complete genomicsTypical
- rs1805794NBN · 89,978,251C;Ccommon in clinvarTypical
- rs1805874CALB1 · 90,069,834A;ANo summary available.Typical
- rs27854193,210,716C;Ccommon genotypeTypical
- rs1835740LOC101927066 · 97,154,685T;Thigher risk for migraine in 1 study which has not replicatedMinor
- rs11996075MATN2 · 97,898,059C;Ccommon in complete genomicsTypical
- rs10107366HRSP12 · 98,101,459T;Tcommon genotypeTypical
- rs4626565COX6C · 99,878,314T;Tcommon/normalTypical
- rs6511SPAG1 · 100,240,452T;Tcommon in clinvarTypical
- rs16867579101,363,039A;Acommon genotypeTypical
- rs16872085104,945,312A;Acommon in complete genomicsTypical
- rs977396RPL23P9 · 104,980,468A;Acommon on affy axiom dataTypical
- rs12678719ZFPM2 · 105,503,826C;Ccommon in complete genomicsTypical
- rs28374544ZFPM2 · 105,802,051A;Acommon in clinvarTypical
- rs7004587107,028,124G;Gcommon genotypeTypical
- rs16892496TRHR · 109,097,622C;C2.7 kg higher lean body massTypical
- rs7832552TRHR · 109,103,447T;T2.55 kg higher lean body massTypical
- rs12549576111,963,912A;Acommon in complete genomicsTypical
- rs17658378115,381,846A;Acommon on affy axiom dataTypical
- rs2293889TRPS1 · 115,586,972T;Tcommon in clinvarTypical
- rs2721937TRPS1 · 115,621,472C;Ccommon in complete genomicsTypical
- rs16892766116,618,444A;Cslight (~1.5x) increase in colorectal cancer riskWorth knowing
- rs16888589116,623,363G;G1.9x higher risk for colorectal cancerWorth knowing
- rs1133950UTP23 · 116,771,675A;Acommon in complete genomicsTypical
- rs13266634SLC30A8 · 117,172,544C;Cincreased risk for type-2 diabetesImportant
- rs3802177SLC30A8 · 117,172,786G;G1.16x increased risk for type-2 diabetesTypical
- rs7459527EXT1 · 117,897,021C;Ccommon genotypeTypical
- rs17749211LOC105375724 · 118,379,170C;CNo summary available.Typical
- rs11988997118,753,955T;TNo summary available.Typical
- rs11573901TNFRSF11B · 118,934,321G;Gcommon in complete genomicsTypical
- rs2073618TNFRSF11B · 118,951,813G;Gcommon in clinvarTypical
- rs2073617TNFRSF11B · 118,952,044G;Gcommon in clinvarTypical
- rs3134069TNFRSF11B · 118,952,749A;ANo summary available.Typical
- rs11989782SNTB1 · 120,682,410A;Ccommon in complete genomicsTypical
- rs956225121,897,448A;Acommon in complete genomicsTypical
- rs10481151123,819,594C;CNo summary available.Minor
- rs11781525MTSS1 · 124,709,125G;Gcommon genotypeTypical
- rs16900305KIAA0196 · 125,061,429G;Gcommon in complete genomicsTypical
- rs1906493126,080,638G;Gcommon in complete genomicsTypical
- rs11986011126,320,412C;Ccommon genotypeTypical
- rs10086908LOC105375751 · 126,999,692C;C1.7x increased risk for prostate cancerWorth knowing
- rs13252298PRNCR1 · 127,082,911A;Acommon in complete genomicsTypical
- rs13254738PRNCR1 · 127,092,098A;C1.18x prostate cancer riskWorth knowing
- rs12682344127,094,539T;Tcommon genotypeTypical
- rs6983561127,094,635A;ANo summary available.Typical
- rs1378897127,110,414C;Ccommon in complete genomicsTypical
- rs16901979127,112,671A;A1.5x increased risk for prostate cancerWorth knowing
- rs10505483127,112,950T;TNo summary available.Typical
- rs138042437CASC19 · 127,196,124A;GModerately higher (2-4 fold?) risk for prostate cancerImportant
- rs16902104CASC8 · 127,328,663C;Ccommon/normalTypical
- rs6983267CASC8 · 127,401,060G;G1.6x increased risk for prostate cancer; also other cancersImportant
- rs6470517CASC8 · 127,448,159A;Acommon in complete genomicsTypical
- rs1447295CASC8 · 127,472,793A;A1.7x increased risk of prostate cancerMinor
- rs10109700CASC8 · 127,473,719G;GNo summary available.Typical
- rs7832031127,504,707G;GNo summary available.Typical
- rs4242382127,505,328A;A1.7x increased risk for prostate cancerWorth knowing
- rs4242384127,506,309A;ANo summary available.Typical
- rs7017300127,513,023A;Anormal riskTypical
- rs10090154127,519,892T;T1.4x increased risk for prostate cancerWorth knowing
- rs7837688127,527,115G;T1.7x increased risk for prostate cancerWorth knowing
- rs9642880CASC11 · 127,705,823G;GSlightly lower risk of Bladder Cancer.Worth knowing
- rs16902460PVT1 · 127,907,951G;Gcommon genotypeTypical
- rs2648875PVT1 · 128,059,915A;A8.82x increased risk of ESRD in diabetes type II patientsTypical
- rs10492294128,234,169T;Tcommon in complete genomicsTypical
- rs9792269128,252,343A;Acommon in complete genomicsTypical
- rs10088218LINC00824 · 128,531,703A;A0.5x decreased risk for ovarian cancerWorth knowing
- rs987525128,933,908A;A6x increased risk for cleft lipWorth knowing
- rs891835CCDC26 · 129,479,506G;GNo summary available.Typical
- rs55705857CCDC26 · 129,633,446A;G6x increased risk of glioma of IDH1/IDH2 subtypeImportant
- rs4295627CCDC26 · 129,673,211G;G1.85x higher risk for glioma developmentMinor
- rs10092658FAM49B · 129,968,226C;Ccommon in complete genomicsTypical
- rs6984045ASAP1 · 130,080,167T;Tcommon in complete genomicsTypical
- rs16904316130,605,604C;Ccommon genotypeTypical
- rs180223TG · 132,888,007G;T1.3x to 11.5x Increased risk of autoimmune thyroid diseaseWorth knowing
- rs2069550TG · 132,888,141T;Tcommon in clinvarTypical
- rs16904774TG · 132,888,250G;Gcommon in clinvarTypical
- rs2229843TG · 132,888,417G;Gcommon in complete genomicsTypical
- rs2069556TG · 132,908,273A;Acommon in clinvarTypical
- rs2069561TG · 132,963,038G;Gcommon in clinvarTypical
- rs2076740TG · 132,971,813C;C2.4-6.1 risk of Autoimmune thyroid disease, if other SNP risk alleles presentWorth knowing
- rs2929973WISP1 · 133,230,265T;Tcommon in complete genomicsTypical
- rs1036819ZFAT · 134,599,702A;Acommon on affy axiom dataTypical
- rs16906293LOC107986980 · 136,756,649C;Ccommon genotypeTypical
- rs2705293LOC401478 · 137,906,702T;Tcommon in complete genomicsTypical
- rs4909764FAM135B · 138,243,675T;Tcommon genotypeTypical
- rs6988229COL22A1 · 138,872,266C;Ccommon in clinvarTypical
- rs6997709139,167,781G;G1.5x higher risk for hypertensionWorth knowing
- rs12679196TRAPPC9 · 139,800,104C;Ccommon in complete genomicsTypical
- rs2294008PSCA · 142,680,513T;Tincreased risk of gastric and bladder cancerWorth knowing
- rs2572886142,821,739A;A1.4x increased risk of HIV infectionWorth knowing
- rs6410CYP11B1 · 142,879,589T;Tcommon in clinvarTypical
- rs104894069CYP11B1 · 142,879,690G;Gcommon in clinvarTypical
- rs3802230CYP11B2 · 142,911,448C;Ccommon in clinvarTypical
- rs3097CYP11B2 · 142,911,899C;Ccommon in clinvarTypical
- rs4545CYP11B2 · 142,912,625C;Ccommon on affy axiom dataTypical
- rs4536CYP11B2 · 142,914,345C;Ccommon in clinvarTypical
- rs1799998CYP11B2 · 142,918,184G;GPossibly higher odds of developing hypertensionWorth knowing
- rs2290416NAPRT · 143,575,430G;Gcommon in complete genomicsTypical
- rs2977838SLC39A4 · 144,415,027G;Gcommon in complete genomicsTypical
- rs17855765SLC39A4 · 144,415,944C;Ccommon in clinvarTypical
- rs2280838SLC39A4 · 144,416,618C;Ccommon in clinvarTypical
- rs1063739LOC101928953 · 144,504,344C;Ccommon in clinvarTypical
- rs2620636ARHGAP39 · 144,552,744C;Ccommon 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.