Chromosome 16
280 well-documented SNPs on chromosome 16, in order of position (GRCh38).
- rs710079MPG · 79,224C;Ccommon in complete genomicsTypical
- rs2541632MPG · 81,110T;Tcommon in complete genomicsTypical
- rs7203560NPRL3 · 134,391T;Tcommon genotypeTypical
- rs41464951HBA2 · 173,598A;TAlpha-thalassemia allele carrierImportant
- rs13339636FAM234A · 248,589A;Acommon genotypeTypical
- rs13335629FAM234A · 260,381G;Gcommon genotypeTypical
- rs3751664CACNA1H · 1,204,369C;Ccommon on affy axiom dataTypical
- rs12926089CLCN7 · 1,452,856C;Ccommon in complete genomicsTypical
- rs28934872TSC2 · 2,070,571A;GTuberous Sclerosis ComplexVery important
- rs45517214TSC2 · 2,072,293G;TTuberous Sclerosis ComplexVery important
- rs13337626TSC2 · 2,075,833T;Tcommon in complete genomicsTypical
- rs777460677PKD1 · 2,093,916-;ACAGCCCarrier of a polycystic kidney disease mutation; inheritance unclearImportant
- rs1057518604PKD1 · 2,103,688-;GPolycystic Kidney Disease likely, but see discussionVery important
- rs1064793762MIR6511B1 · 2,108,254A;GPolycystic Kidney Disease likely, but see discussionVery important
- rs1064794207PKD1 · 2,116,564A;GPolycystic Kidney Disease likely, but see discussionVery important
- rs58598099PKD1 · 2,116,917A;GVery likely just a miscall due to pseudogenes; but if it were accurate, dominant polycystic kidney genotypeTypical
- rs149989682ABCA3 · 2,317,763A;ASurfactant metabolism dysfunction, pulmonary, 3; severe neonatal conditionVery important
- rs28940579MEFV · 3,243,310G;Gfamilial Mediterranean feverImportant
- rs104895094MEFV · 3,243,403C;CFamilial Mediterranean Fever, autosomal recessiveVery important
- rs28940578MEFV · 3,243,405T;Tfamilial Mediterranean feverImportant
- rs61752717MEFV · 3,243,407C;Cfamilial mediterranean feverVery important
- rs28940580MEFV · 3,243,447C;GFamilial mediterranean fever (predicted)Very important
- rs104895083MEFV · 3,247,166C;GCarrier of a familial mediterranean fever mutationImportant
- rs11466026MEFV · 3,248,947G;Gcommon in clinvarTypical
- rs11466024MEFV · 3,249,468T;TbenignMinor
- rs11466023MEFV · 3,249,586A;Amild familial Mediterranean feverWorth knowing
- rs3743930MEFV · 3,254,626G;Gsome reports of familial Mediterranean feverWorth knowing
- rs8176927DNASE1 · 3,655,379G;Gcommon in complete genomicsTypical
- rs3751845CREBBP · 3,728,336G;Gcommon in clinvarTypical
- rs129974CREBBP · 3,745,291G;Gcommon in complete genomicsTypical
- rs3025684CREBBP · 3,745,362G;Gcommon in complete genomicsTypical
- rs130002CREBBP · 3,777,930T;Tcommon in complete genomicsTypical
- rs11644721CREBBP · 3,851,010C;Ccommon in clinvarTypical
- rs1045643UBN1 · 4,881,512C;Ccommon in complete genomicsTypical
- rs17139207A2BP1 · 6,036,271A;Acommon in complete genomicsTypical
- rs9302841A2BP1 · 7,177,121T;Tcommon in complete genomicsTypical
- rs4787008RBFOX1 · 7,365,551G;Gcommon on affy axiom dataTypical
- rs20345888,279,325T;Tcommon in complete genomicsTypical
- rs1731017ABAT · 8,746,097A;Acommon in clinvarTypical
- rs11146209,169,880T;Tcommon in complete genomicsTypical
- rs13335336ATF7IP2 · 10,465,406A;Acommon in complete genomicsTypical
- rs8048002LOC105371080 · 10,898,131T;Tcommon in complete genomicsTypical
- rs8046121LOC105371080 · 10,902,076A;Acommon in clinvarTypical
- rs4774LOC105371080 · 10,906,991G;Gcommon in clinvarTypical
- rs7197779LOC105371080 · 10,909,070A;Acommon in clinvarTypical
- rs725613CLEC16A · 11,075,826T;T1.2x increased type-1 diabetes risk; 1.2x increased multiple sclerosis riskTypical
- rs12708716CLEC16A · 11,086,016A;A1.6x risk of type-1 diabetesTypical
- rs6498169CLEC16A · 11,155,472A;A>1.14x risk of multiple sclerosisWorth knowing
- rs33977706LOC105371082 · 11,256,298A;ALower body mass indexWorth knowing
- rs2301365PRM1 · 11,281,429G;Gcommon/normalTypical
- rs12928822LOC105371082 · 11,310,036C;Ccommon on affy axiom dataTypical
- rs4280262LITAF · 11,553,636T;Tcommon in clinvarTypical
- rs373496TNFRSF17 · 11,966,306G;Gcommon in complete genomicsTypical
- rs1641895SNX29 · 12,547,258C;Ccommon genotypeTypical
- rs254942ERCC4 · 13,932,150G;Gcommon in clinvarTypical
- rs1800067ERCC4 · 13,935,176A;GNo summary available.Typical
- rs2020955ERCC4 · 13,944,802T;Tcommon in complete genomicsTypical
- rs1799801ERCC4 · 13,948,101T;Tcommon in clinvarTypical
- rs1800124ERCC4 · 13,948,220A;Acommon in clinvarTypical
- rs2276465ERCC4 · 13,949,157G;Gcommon in clinvarTypical
- rs2276466ERCC4 · 13,949,318C;Ccommon in clinvarTypical
- rs4781563ERCC4 · 13,951,542G;Gcommon in clinvarTypical
- rs3765129ABCC1 · 16,056,044C;CNo summary available.Typical
- rs35623ABCC1 · 16,075,608G;Gcommon in clinvarTypical
- rs4148351ABCC1 · 16,076,711C;Ccommon in clinvarTypical
- rs35626ABCC1 · 16,076,758G;Gcommon in clinvarTypical
- rs4148356ABCC1 · 16,083,418G;Gcommon in complete genomicsTypical
- rs2238476ABCC1 · 16,120,015G;GNo summary available.Typical
- rs4148382ABCC1 · 16,144,637G;Gcommon in complete genomicsTypical
- rs2238472ABCC6 · 16,157,742T;Tmost likely a benign polymorphismMinor
- rs150468ABCC6 · 16,158,143T;Tcommon in complete genomicsTypical
- rs2856585ABCC6 · 16,169,806G;Gcommon in clinvarTypical
- rs11861980ABCC6 · 16,173,376G;Gcommon in clinvarTypical
- rs9924755ABCC6 · 16,177,552G;Gcommon in clinvarTypical
- rs7500834ABCC6 · 16,178,813C;Ccommon in complete genomicsTypical
- rs4341770ABCC6 · 16,182,880A;Acommon in clinvarTypical
- rs212077ABCC6 · 16,186,919G;Gcommon in complete genomicsTypical
- rs806232619,144,694G;Gcommon in complete genomicsTypical
- rs1259757920,246,545C;Ccommon in complete genomicsTypical
- rs4078023GP2 · 20,308,765T;TNo summary available.Typical
- rs11859916UMOD · 20,339,909G;Gcommon in complete genomicsTypical
- rs4293393UMOD · 20,353,266G;G0.76x reduced risk of CKD for C alleleTypical
- rs13333226UMOD · 20,354,332G;G~15-20% lower risk for hypertension or cardiovascular eventsMinor
- rs12917707UMOD · 20,356,368G;Gcommon on affy axiom dataTypical
- rs151222ACSM1 · 20,663,170G;Gcommon on affy axiom dataTypical
- rs16970881DNAH3 · 21,101,951G;Gcommon genotypeTypical
- rs11648723UQCRC2 · 21,974,165G;Gcommon/normalTypical
- rs5736SCNN1G · 23,189,600G;Gcommon in clinvarTypical
- rs5738SCNN1G · 23,189,642G;Gcommon in clinvarTypical
- rs447529PALB2 · 23,622,102G;GBenign variantTypical
- rs420259PALB2 · 23,622,705G;GHalf the risk of developing Bipolar Disorder.Minor
- rs249954PALB2 · 23,629,146A;APotentially increased risk of Breast CancerMinor
- rs16940342PALB2 · 23,633,265A;Acommon in clinvarTypical
- rs180177102PALB2 · 23,634,954-;-Fanconi anemia, complementation group NVery important
- rs8053188PALB2 · 23,641,204C;Ccommon in complete genomicsTypical
- rs4968031CHP2 · 23,754,453G;Gcommon in complete genomicsTypical
- rs1164352024,520,397T;Tcommon in complete genomicsTypical
- rs17177078TNRC6A · 24,799,360C;Ccommon genotypeTypical
- rs720126825,401,045G;GNo summary available.Typical
- rs16976587KDM8 · 27,203,663G;Gcommon genotypeTypical
- rs1805010IL4R · 27,344,882A;Acommon in clinvarTypical
- rs1805012IL4R · 27,362,643T;Tcommon on affy axiom dataTypical
- rs1805013IL4R · 27,362,659C;Ccommon in complete genomicsTypical
- rs17513769IL4R · 27,362,859T;TNo summary available.Typical
- rs1801275IL4R · 27,363,079A;ANo summary available.Typical
- rs1805016IL4R · 27,363,606T;TNo summary available.Typical
- rs4788099TUFM · 28,844,406A;Acommon in clinvarTypical
- rs2904880CD19 · 28,933,075C;Ccommon in clinvarTypical
- rs35979293CD19 · 28,933,379G;Gcommon in clinvarTypical
- rs2289292TBX6 · 30,086,309C;Ccommon in clinvarTypical
- rs3809624TBX6 · 30,091,481T;Tcommon in clinvarTypical
- rs572115942PHKG2 · 30,756,714A;GIn type-1 diabetics (only), Mauriac syndrome predictedVery important
- rs1046276CTF1 · 30,903,305T;Tcommon in clinvarTypical
- rs9938550HSD3B7 · 30,987,821A;Acommon in clinvarTypical
- rs7294PRSS53 · 31,091,000C;Ccommon in clinvarTypical
- rs7200749PRSS53 · 31,091,268G;Gcommon in complete genomicsTypical
- rs2359612VKORC1 · 31,092,475A;Acommon in clinvarTypical
- rs8050894VKORC1 · 31,093,188C;Cwarfarin sensitivity (~2.5 mg/day)Worth knowing
- rs9934438VKORC1 · 31,093,557A;Acoumadin resistanceWorth knowing
- rs17708472VKORC1 · 31,094,032G;Gcommon in clinvarTypical
- rs2884737VKORC1 · 31,094,233A;Acommon in clinvarTypical
- rs9923231VKORC1 · 31,096,368T;Treduced warfarin dose if treated for VTEWorth knowing
- rs12597511PRSS8 · 31,133,898C;CnormalTypical
- rs741810FUS · 31,182,621C;Ccommon in clinvarTypical
- rs1052352FUS · 31,183,958C;Ccommon in clinvarTypical
- rs121909667FUS · 31,191,408G;GCausing ALS AMYOTROPHIC LATERAL SCLEROSISVery important
- rs9888739ITGAM · 31,301,932C;CNo summary available.Typical
- rs61742739SLC5A2 · 31,490,477G;Grenal glycosuria possible, but see discussionWorth knowing
- rs12918964PHKB · 47,698,565C;Ccommon in complete genomicsTypical
- rs17822931ABCC11 · 48,224,287T;TDry earwax. No body odour. Likely Asian ancestry. Reduced colostrum.Worth knowing
- rs3901517BRD7 · 50,357,475C;CNo summary available.Typical
- rs2067085NOD2 · 50,699,948C;Ccommon in clinvarTypical
- rs17221417NOD2 · 50,705,671G;G1.9x higher risk for Crohn's diseaseWorth knowing
- rs2066842NOD2 · 50,710,713C;Ccommon in clinvarTypical
- rs2066843NOD2 · 50,711,288T;T4.09x higher risk for Crohn's diseaseWorth knowing
- rs2066844NOD2 · 50,712,015T;TSignificance unclear; possibly higher risk for Crohn's diseaseImportant
- rs5743277NOD2 · 50,712,018C;Ccommon in clinvarTypical
- rs2066845NOD2 · 50,722,629C;C~35x higher risk for Crohn's diseaseVery important
- rs5743289NOD2 · 50,722,863C;TPerhaps increased risk for certain autoinflammatory disordersMinor
- rs2076756NOD2 · 50,722,970A;AnormalTypical
- rs3135499NOD2 · 50,732,216A;Acommon in clinvarTypical
- rs3135500NOD2 · 50,732,975G;Gcommon in clinvarTypical
- rs1052122251,124,799C;Ccommon in complete genomicsTypical
- rs4614723SALL1 · 51,137,264C;Ccommon in clinvarTypical
- rs1695102152,288,064T;Tcommon genotypeTypical
- rs8051542TOX3 · 52,500,255C;Ccommon/normalTypical
- rs3803662CASC16 · 52,552,429A;A1.6x increased risk for breast cancerImportant
- rs134448452,878,387C;CnormalTypical
- rs4784319RPGRIP1L · 53,602,021A;Acommon in clinvarTypical
- rs9922369RPGRIP1L · 53,614,570G;Gcommon in complete genomicsTypical
- rs1421085FTO · 53,767,042C;C~1.7x increased obesity riskImportant
- rs1558902FTO · 53,769,662A;AHigher BMI than normalTypical
- rs1121980FTO · 53,775,335A;AModerate increase (2.76x) in risk for obesityImportant
- rs16945088FTO · 53,778,612A;ANo summary available.Typical
- rs17817449FTO · 53,779,455G;G~1.7x increased obesity riskTypical
- rs8050136FTO · 53,782,363A;A1.4x increased risk for T2D in some populationsMinor
- rs3751812FTO · 53,784,548G;GnormalTypical
- rs9939609FTO · 53,786,615A;Aobesity risk and 1.6x risk for T2DImportant
- rs9930506FTO · 53,796,553A;AnormalTypical
- rs7204609FTO · 53,799,693T;Tcommon in complete genomicsTypical
- rs7195539FTO · 53,825,246A;Acommon genotypeTypical
- rs16953002FTO · 54,080,912A;A1.32x increased risk of melanoma in those with low BMIMinor
- rs719919654,315,695T;Tcommon genotypeTypical
- rs243866MMP2 · 55,477,625G;GNo summary available.Typical
- rs2287074MMP2 · 55,493,201G;Gcommon in clinvarTypical
- rs7201MMP2 · 55,505,702A;Acommon in clinvarTypical
- rs2242446SLC6A2 · 55,656,513C;Ccommon in clinvarTypical
- rs3785143SLC6A2 · 55,661,194C;Tmay be associated with ADHDMinor
- rs734980SLC6A2 · 55,668,637A;Acommon in complete genomicsTypical
- rs187715SLC6A2 · 55,670,130T;TNo summary available.Typical
- rs3785152SLC6A2 · 55,682,638C;Ccommon in complete genomicsTypical
- rs3785155SLC6A2 · 55,688,478G;GNo summary available.Typical
- rs11568324SLC6A2 · 55,692,146C;Ccommon in complete genomicsTypical
- rs5568SLC6A2 · 55,696,212A;Acommon in clinvarTypical
- rs5569SLC6A2 · 55,697,923G;Gcommon in clinvarTypical
- rs998424SLC6A2 · 55,698,034G;Gcommon in clinvarTypical
- rs5558SLC6A2 · 55,699,647A;ANo summary available.Typical
- rs7194256SLC6A2 · 55,703,779C;Ccommon in clinvarTypical
- rs4784677BBS2 · 56,514,589C;Ccommon in clinvarTypical
- rs396230MT4 · 56,568,704T;Tcommon in complete genomicsTypical
- rs9936741MT1M · 56,633,873T;Tcommon genotypeTypical
- rs1529927SLC12A3 · 56,870,675G;Gcommon in complete genomicsTypical
- rs13306668SLC12A3 · 56,879,088G;Gcommon in clinvarTypical
- rs12708965SLC12A3 · 56,902,407C;Ccommon in complete genomicsTypical
- rs376426156,959,412A;Aassociated with higher HDL cholesterol. HDL = goodWorth knowing
- rs708272CETP · 56,962,376A;AB2B2 genotype; some reduction in heart disease risk from moderate alcohol consumptionWorth knowing
- rs1864163CETP · 56,963,321A;Gassociated with higher HDL cholesterolWorth knowing
- rs1532624CETP · 56,971,567C;Ccommon in clinvarTypical
- rs5880CETP · 56,981,179G;Gcommon in complete genomicsTypical
- rs5882CETP · 56,982,180G;GLonger lifespan, 0.28x lower risk of dementia, 0.31x lower risk of Alzheimer's.Worth knowing
- rs2303790CETP · 56,983,380A;Acommon in clinvarTypical
- rs1566439NLRC5 · 56,990,750G;Gassociated with higher HDL cholesterolWorth knowing
- rs16965039NLRC5 · 57,013,387T;Tcommon in complete genomicsTypical
- rs4359426CCL22 · 57,358,821C;Ccommon genotypeTypical
- rs1782211460,699,699C;CNo summary available.Typical
- rs805094062,066,307T;Tcommon genotypeTypical
- rs1696775364,601,500C;Ccommon genotypeTypical
- rs9939768EXOC3L1 · 67,185,204G;Gcommon in complete genomicsTypical
- rs868213EXOC3L · 67,186,554A;Acommon in complete genomicsTypical
- rs3729639E2F4 · 67,191,598C;Ccommon in complete genomicsTypical
- rs5479HSD11B2 · 67,435,830C;Ccommon in complete genomicsTypical
- rs28937570AGRP · 67,483,042C;CNo summary available.Typical
- rs5030980ATP6V0D1 · 67,483,042C;Ccommon in complete genomicsTypical
- rs34123523AGRP · 67,483,276C;Ccommon in complete genomicsTypical
- rs2271293NUTF2 · 67,868,167G;Gcommon on affy axiom dataTypical
- rs11574514PSMB10 · 67,937,477C;Ccommon in complete genomicsTypical
- rs5923LCAT · 67,940,050G;Gcommon in clinvarTypical
- rs4986970LCAT · 67,942,417A;Acommon in complete genomicsTypical
- rs255049DPEP3 · 67,979,568T;TNo summary available.Typical
- rs255052DPEP2 · 67,991,092G;GNo summary available.Typical
- rs16260CDH1 · 68,737,131A;A2.6x increased risk of prostate cancerTypical
- rs121964875CDH1 · 68,738,307A;GLikely miscall, at least by Ancestry and possibly by 23andMe; otherwise, Hereditary cancer-predisposing syndrome; gastric cancer relatedVery important
- rs121964876CDH1 · 68,738,318G;TFalse positives possible; otherwise, Hereditary cancer-predisposing syndromeVery important
- rs1801552CDH1 · 68,823,538T;Tcommon in clinvarTypical
- rs13689CDH1 · 68,834,619T;Tcommon in clinvarTypical
- rs2232228HAS3 · 69,109,674A;Acommon in clinvarTypical
- rs1800566NQO1 · 69,711,242A;ABenzene toxicity; cancer risksImportant
- rs1131341NQO1 · 69,714,966G;GNo summary available.Typical
- rs875858VAC14 · 70,741,552T;Tdocetaxel sensitive?Very important
- rs9938025PKD1L3 · 71,988,142A;ALower odds of dry earwax in Europeans.Worth knowing
- rs3213422DHODH · 72,008,783A;Acommon in clinvarTypical
- rs5470TXNL4B · 72,054,522C;Ccommon in complete genomicsTypical
- rs2106261ZFHX3 · 73,017,721C;Ccommon/normalTypical
- rs12446956C16orf47 · 73,467,637T;Tcommon on affy axiom dataTypical
- rs1694825574,847,922C;Ccommon in complete genomicsTypical
- rs7190458BCAR1 · 75,229,763A;AHigher pancreatic cancer riskWorth knowing
- rs4888378CFDP1 · 75,298,143A;AFor women, slower carotid thickening with age (so presumably lower atherosclerotic risk)Worth knowing
- rs198295576,935,701T;Tcommon genotypeTypical
- rs11864477ADAMTS18 · 77,393,872T;TNo summary available.Typical
- rs11545028WWOX · 78,099,774C;Ccommon in clinvarTypical
- rs11545029WWOX · 78,386,878G;Gcommon in clinvarTypical
- rs3764340WWOX · 78,432,540C;Ccommon in clinvarTypical
- rs17706989WWOX · 78,536,060C;Ccommon on affy axiom dataTypical
- rs2859631WWOX · 78,597,897A;Acommon in complete genomicsTypical
- rs9923451WWOX · 78,918,542G;Gcommon in complete genomicsTypical
- rs17713676WWOX · 79,039,524C;Ccommon genotypeTypical
- rs383362MAF · 79,211,923G;GnormalTypical
- rs17797882MAF · 79,373,021C;Ccommon in complete genomicsTypical
- rs4888966MAF · 79,397,956C;Ccommon genotypeTypical
- rs7498403MAF · 79,551,124T;Tcommon in complete genomicsTypical
- rs656485181,230,992G;Ghigher beta-carotene levelsTypical
- rs12934922BCO1 · 81,268,089A;TReduced conversion of beta-carotene to retinolMinor
- rs7501331BCO1 · 81,280,891C;TReduced conversion of beta-carotene to retinolWorth knowing
- rs2608555GAN · 81,365,030C;Ccommon in clinvarTypical
- rs16955379CMIP · 81,455,768C;Ccommon in complete genomicsTypical
- rs72824905PLCG2 · 81,908,423C;GModerate decrease (~0.6x) in risk for Alzheimer's disease as well as FTD and DLBImportant
- rs1424151HSD17B2 · 82,095,747A;Acommon in complete genomicsTypical
- rs1186306582,293,200G;Gcommon genotypeTypical
- rs408251482,346,348G;Gcommon on affy axiom dataTypical
- rs4783244CDH13 · 82,628,663G;GNormalTypical
- rs12051272CDH13 · 82,629,683G;Gcommon in complete genomicsTypical
- rs11646411CDH13 · 82,713,332C;Ccommon in complete genomicsTypical
- rs12386026CDH13 · 82,783,986C;Ccommon in complete genomicsTypical
- rs6565105CDH13 · 83,032,059G;Gcommon in clinvarTypical
- rs8055236CDH13 · 83,178,793G;Gcommon, but 2.2x higher risk for heart diseaseMinor
- rs17216786CDH13 · 83,453,866C;Ccommon in complete genomicsTypical
- rs9939760CDH13 · 83,619,297G;Gcommon genotypeTypical
- rs1048612CDH13 · 83,783,414A;Acommon in clinvarTypical
- rs4150167TAF1C · 84,180,078C;Ccommon genotypeTypical
- rs16963349WFDC1 · 84,304,628T;Tcommon genotypeTypical
- rs2696835LINC00917 · 86,331,965G;Gcommon in complete genomicsTypical
- rs1164498886,451,525G;Gcommon genotypeTypical
- rs1694183586,662,114G;Gcommon/normalTypical
- rs757972971SLC7A5 · 87,837,861A;APossible autism spectrum disorder genotypeVery important
- rs4673CYBA · 88,646,828A;AConflicting impact reported wrt heart disease risk; may depend on ethnicityMinor
- rs202103485LOC100289580 · 88,733,652C;TXerocytosis-associated according to literature, but probably actually of little consequenceMinor
- rs200970763LOC100289580 · 88,733,731C;TXerocytosis-associated according to literature, but probably actually of little consequenceMinor
- rs2292954SPG7 · 89,546,715A;Acommon on affy axiom dataTypical
- rs61755320SPG7 · 89,546,737T;TSpastic paraplegia, type 7; however, possibly reduced penetranceVery important
- rs12960SPG7 · 89,553,920G;Gcommon in clinvarTypical
- rs258322CDK10 · 89,689,495A;A2x increased risk of MelanomaImportant
- rs1061646FANCA · 89,739,569G;G1.16x increased risk for breast cancerTypical
- rs16966142FANCA · 89,784,625C;Ccommon in complete genomicsTypical
- rs7190823FANCA · 89,799,635T;Tcommon in clinvarTypical
- rs1805005MC1R · 89,919,436G;Gcommon in clinvarTypical
- rs2228479MC1R · 89,919,532G;Gcommon in clinvarTypical
- rs1805007MC1R · 89,919,709T;Tincreased response to anesthetics; 13-20x higher likelihood of red hair; increased risk of melanomaImportant
- rs1805008MC1R · 89,919,736T;T~7-10x higher likelihood of red hair; higher risk of melanomaImportant
- rs885479MC1R · 89,919,746A;Alighter skin colorWorth knowing
- rs4785763AFG3L1 · 90,000,528A;A2x higher risk for melanomaMinor
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.