Chromosome 4
341 well-documented SNPs on chromosome 4, in order of position (GRCh38).
- rs10902758LOC101928521 · 654,854A;Acommon in complete genomicsTypical
- rs4234853PCGF3 · 741,362G;Gcommon in complete genomicsTypical
- rs1564282GAK · 858,525C;Ccommon on affy axiom dataTypical
- rs11248051GAK · 864,544C;Ccommon on affy axiom dataTypical
- rs11248060DGKQ · 970,571C;Ccommon on affy axiom dataTypical
- rs3755955IDUA · 1,000,626G;Gcommon in clinvarTypical
- rs6831280IDUA · 1,002,377G;Gcommon in clinvarTypical
- rs7656416MAEA · 1,260,747C;Ccommon in complete genomicsTypical
- rs6815464MAEA · 1,316,113C;Ccommon in complete genomicsTypical
- rs798766TACC3 · 1,732,512T;TIncreased susceptibility urinary bladder cancerMinor
- rs2234909FGFR3 · 1,801,977T;Tcommon in clinvarTypical
- rs77722678FGFR3 · 1,805,643G;GHypochondroplasiaVery important
- rs4961ADD1 · 2,904,980T;T1.8x increased risk for high blood pressureWorth knowing
- rs2960306GRK4 · 2,988,772G;Gcommon in complete genomicsTypical
- rs1143646HTT · 3,146,926T;Tcommon in complete genomicsTypical
- rs1447285STK32B · 5,083,198T;Tcommon in complete genomicsTypical
- rs730469EVC2 · 5,622,943T;Tcommon in clinvarTypical
- rs4689278EVC2 · 5,689,175T;Tcommon in complete genomicsTypical
- rs6414624EVC · 5,741,785C;CNo summary available.Typical
- rs35953626EVC · 5,753,797G;Gcommon in clinvarTypical
- rs2302075EVC · 5,753,815T;TNo summary available.Typical
- rs1383180EVC · 5,783,715G;Gcommon in clinvarTypical
- rs16838131JAKMIP1 · 6,056,770G;Gcommon genotypeTypical
- rs71530923WFS1 · 6,277,579C;Ccommon in clinvarTypical
- rs6446482WFS1 · 6,293,966C;Ccommon in clinvarTypical
- rs1801212WFS1 · 6,300,792G;Gcommon in clinvarTypical
- rs1801208WFS1 · 6,301,162G;Gcommon in clinvarTypical
- rs1046320LOC107986257 · 6,302,617G;Gcommon in clinvarTypical
- rs16839553TBC1D14 · 7,016,458G;Gcommon genotypeTypical
- rs10937823SORCS2 · 7,478,695C;Tsome association with bipolar disorderWorth knowing
- rs4696688AFAP1 · 7,938,188G;Gcommon in complete genomicsTypical
- rs2227852DRD5 · 9,782,741A;ANo summary available.Minor
- rs1850744SLC2A9 · 9,789,088C;CNo summary available.Typical
- rs3733591SLC2A9 · 9,920,506C;Ccommon in clinvarTypical
- rs16890979SLC2A9 · 9,920,543T;Tlower systolic blood pressure, serum uric acid and gout riskWorth knowing
- rs6855911SLC2A9 · 9,934,286A;Anormal, but increased risk of goutWorth knowing
- rs12498742SLC2A9 · 9,942,428A;A1.25 increased risk for goutMinor
- rs7442295SLC2A9 · 9,964,756A;A~4x higher risk for hyperuracemiaWorth knowing
- rs6449213LOC105374476 · 9,992,591C;C~4x higher risk for hyperuracemiaWorth knowing
- rs3775948LOC105374476 · 9,993,558C;Cslightly higher risk for goutWorth knowing
- rs13113918LOC105374476 · 9,996,869A;Acommon in clinvarTypical
- rs1251054910,274,843C;CDecreased risk for high uric acid levels and goutMinor
- rs7665957LOC105374492 · 12,497,263C;Ccommon genotypeTypical
- rs205611613,008,363G;G1.41x risk for breast cancerWorth knowing
- rs49137613,115,138C;Ccommon in complete genomicsTypical
- rs57333213,120,911T;Tcommon in complete genomicsTypical
- rs10489087LOC101929048 · 13,792,792G;Gcommon in complete genomicsTypical
- rs16891867C1QTNF7 · 15,395,740A;Acommon genotypeTypical
- rs1861046C1QTNF7 · 15,396,282G;GNo summary available.Minor
- rs1861050CC2D2A · 15,480,736C;Ccommon in complete genomicsTypical
- rs16892095CC2D2A · 15,516,734A;Acommon genotypeTypical
- rs12502586BST1 · 15,724,941G;Gcommon in complete genomicsTypical
- rs4538475BST1 · 15,736,314G;GIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs3130PROM1 · 15,968,315T;Tcommon in clinvarTypical
- rs2240688PROM1 · 15,968,726T;Tcommon in clinvarTypical
- rs2286455PROM1 · 16,018,539C;Ccommon in clinvarTypical
- rs469816917,133,720C;Ccommon in complete genomicsTypical
- rs7678436DCAF16 · 17,796,343G;Gcommon in complete genomicsTypical
- rs6817306LCORL · 17,866,435T;Tcommon in complete genomicsTypical
- rs16896068LCORL · 17,943,217G;Gcommon in complete genomicsTypical
- rs6830062LCORL · 18,016,107T;Tcommon in complete genomicsTypical
- rs1379659SLIT2 · 20,619,060A;Acommon on affy axiom dataTypical
- rs16871289KCNIP4 · 21,509,760C;Ccommon genotypeTypical
- rs1687224822,019,877C;Ccommon genotypeTypical
- rs3774923PPARGC1A · 23,793,441C;CNo summary available.Typical
- rs3736265PPARGC1A · 23,813,084G;GNo summary available.Typical
- rs8192678PPARGC1A · 23,814,039T;Thigher blood pressure if <50Typical
- rs7656250PPARGC1A · 23,864,393T;Tcommon in complete genomicsTypical
- rs13117172PPARGC1A · 23,878,892C;Ccommon in complete genomicsTypical
- rs17650401PPARGC1A · 24,374,210C;Ccommon genotypeTypical
- rs769825024,514,008C;Ccommon genotypeTypical
- rs6841898DHX15 · 24,576,474C;Ccommon genotypeTypical
- rs8192287SOD3 · 24,794,946G;GnormalTypical
- rs8192288SOD3 · 24,795,056G;GnormalTypical
- rs699473SOD3 · 24,795,181C;C~1.5x increased brain tumor riskMinor
- rs1799895SOD3 · 24,800,212G;GLower risk for lung disease; Higher risk for ischemic heart diseaseWorth knowing
- rs1553153SEPSECS · 25,147,343C;Ccommon/normalTypical
- rs16877106ANAPC4 · 25,401,644C;Ccommon in complete genomicsTypical
- rs3816587ANAPC4 · 25,415,622C;C1.3x riskTypical
- rs685170227,054,735A;Acommon in complete genomicsTypical
- rs144828433,078,033A;Acommon genotypeTypical
- rs1051727033,201,518G;Gcommon in complete genomicsTypical
- rs683448335,981,489T;Tcommon genotypeTypical
- rs10029345DTHD1 · 36,280,215G;Gcommon in complete genomicsTypical
- rs1311781637,062,709G;Gcommon in complete genomicsTypical
- rs35859249TBC1D1 · 37,902,468C;CnormalTypical
- rs1000849238,764,099C;CnormalTypical
- rs4129009TLR10 · 38,773,268T;Tcommon in complete genomicsTypical
- rs11466653TLR10 · 38,774,614A;Acommon genotypeTypical
- rs5743613TLR1 · 38,797,888G;Gcommon in complete genomicsTypical
- rs5743592TLR1 · 38,801,442A;Acommon in complete genomicsTypical
- rs483310338,813,881A;AnormalTypical
- rs5743815TLR6 · 38,828,194A;Acommon in complete genomicsTypical
- rs5743809TLR6 · 38,828,893A;GCarrier of a likely mutation for Kawasaki diseaseImportant
- rs35141484KLHL5 · 39,086,721A;Acommon genotypeTypical
- rs17585937LOC344967 · 40,044,067C;CNo summary available.Typical
- rs682337941,709,845T;Tcommon in complete genomicsTypical
- rs16853571LOC105374425 · 41,751,113A;Acommon in complete genomicsTypical
- rs1051713345,362,897G;Gcommon in complete genomicsTypical
- rs279858GABRA2 · 46,312,576C;Capparently more prone to alcoholismWorth knowing
- rs16859788GABRA4 · 46,969,992A;Acommon in complete genomicsTypical
- rs16859834GABRA4 · 46,993,349G;GNo summary available.Typical
- rs2351299GABRB1 · 47,141,348G;Gnormal risk of autismMinor
- rs11725957CWH43 · 49,060,875G;Gcommon in complete genomicsTypical
- rs1769023254,368,658C;Ccommon in complete genomicsTypical
- rs2125489KDR · 55,087,316G;Gcommon in complete genomicsTypical
- rs1870377KDR · 55,106,807T;Tcommon in clinvarTypical
- rs2305948KDR · 55,113,391C;Ccommon in complete genomicsTypical
- rs1801260CLOCK · 55,435,202G;GLower ADHD symptom scores.Worth knowing
- rs3736544CLOCK · 55,443,825G;Gcommon/normalTypical
- rs1554483CLOCK · 55,455,650C;CnormalTypical
- rs4864548CLOCK · 55,547,636A;AnormalTypical
- rs629242KIAA1211 · 56,276,871T;Tsomewhat higher risk for prostate cancerWorth knowing
- rs12505749LOC107986282 · 56,467,946C;Ccommon genotypeTypical
- rs1713985REST · 56,920,284T;Tcommon in complete genomicsTypical
- rs2227902REST · 56,930,934G;Gcommon in complete genomicsTypical
- rs3796530REST · 56,931,087G;Gcommon in complete genomicsTypical
- rs3796529REST · 56,931,248T;TNo summary available.Typical
- rs1721816158,347,679T;Tcommon genotypeTypical
- rs6856328ADGRL3 · 61,571,600C;Ccommon in complete genomicsTypical
- rs1155865LOC105377262 · 66,868,139A;Acommon in complete genomicsTypical
- rs1038426GNRHR · 67,737,817C;Ccommon in clinvarTypical
- rs13138607GNRHR · 67,755,832G;Gcommon in clinvarTypical
- rs13327941UGT2B17 · 68,556,427C;Ccommon in complete genomicsTypical
- rs11938019UGT2B17 · 68,559,644C;Ccommon in complete genomicsTypical
- rs7436338UGT2B17 · 68,567,561G;Gcommon in complete genomicsTypical
- rs6857249UGT2B17 · 68,569,184A;Acommon in complete genomicsTypical
- rs12233719UGT2B7 · 69,096,731G;Gcommon in complete genomicsTypical
- rs17147990HTN3 · 70,033,205T;Tcommon in clinvarTypical
- rs3796704ENAM · 70,643,714G;Gcommon in clinvarTypical
- rs3775289DCK · 70,996,957C;Ccommon genotypeTypical
- rs2282679GC · 71,742,666G;Glower vitamin D levelsMinor
- rs4588GC · 71,752,606G;Gcommon in clinvarTypical
- rs7041GC · 71,752,617A;Aex-smokers at 2x higher risk for COPD; supplement with Vitamin D?Minor
- rs4752GC · 71,756,849A;Acommon in complete genomicsTypical
- rs222020GC · 71,770,555T;TNo summary available.Typical
- rs3733359GC · 71,784,057G;Gcommon in complete genomicsTypical
- rs6818964ANKRD17 · 73,104,747C;Ccommon genotypeTypical
- rs2227532IL8 · 73,739,815T;Tcommon in complete genomicsTypical
- rs16850864LOC105377276 · 74,295,107C;Ccommon genotypeTypical
- rs16850885LOC105377276 · 74,304,423G;Gcommon genotypeTypical
- rs216888974,357,994A;Acommon genotypeTypical
- rs3733236LOC101928809 · 76,002,845G;Gcommon in complete genomicsTypical
- rs35795399ART3 · 76,021,524T;TNo summary available.Typical
- rs6836703ART3 · 76,108,994A;A1.34x increased risk for azoospermia in malesTypical
- rs6812193FAM47E-STBD1 · 76,277,833T;TSlightly decreased risk of developing Parkinson's DiseaseMinor
- rs17319721SHROOM3 · 76,447,694A;Areported to have some negative associations with kidney functionMinor
- rs1700225376,850,192T;Tcommon in complete genomicsTypical
- rs17002342LOC105377291 · 77,034,052T;Tcommon genotypeTypical
- rs2288255BMP2K · 78,865,702G;Gcommon in complete genomicsTypical
- rs12507099BMP2K · 78,911,552C;Ccommon on affy axiom dataTypical
- rs13140055ANTXR2 · 80,072,642G;Gcommon in clinvarTypical
- rs3796804PRKG2 · 81,088,553G;Gcommon in complete genomicsTypical
- rs6837293PRKG2 · 81,141,777T;TIf Taiwanese, you might be 2.72 times more likely to develop goutWorth knowing
- rs7688672PRKG2 · 81,148,295A;AIf Taiwanese, you might be ~3x more likely to develop goutWorth knowing
- rs7658637RNASE1 · 82,578,160C;Ccommon in complete genomicsTypical
- rs6535454COQ2 · 83,269,878A;A2x odds of myopathy if taking statinsWorth knowing
- rs4693075COQ2 · 83,271,015G;G2x odds of myopathy if taking statinsWorth knowing
- rs2230600PTPN13 · 86,769,845G;GNo summary available.Minor
- rs10050311SLC10A6 · 86,833,266C;Ccommon/normalTypical
- rs72613567HSD17B13 · 87,310,240A;ALower risk (~1/2 roughly) for chronic liver diseaseImportant
- rs10019009DMP1 · 87,661,983A;Acommon in clinvarTypical
- rs7698623MEPE · 87,834,676C;Ccommon in complete genomicsTypical
- rs1264443687,884,056A;Gcommon in complete genomicsTypical
- rs1481012ABCG2 · 88,117,930A;Acommon in complete genomicsTypical
- rs2199936ABCG2 · 88,124,179A;ANo summary available.Typical
- rs2231142ABCG2 · 88,131,171T;Tcauses goutImportant
- rs72552713ABCG2 · 88,131,805A;AHigher risk for goutImportant
- rs2231137ABCG2 · 88,139,962T;TSlightly lower stroke riskMinor
- rs3114018ABCG2 · 88,143,429A;CSomewhat higher risk for gout among ChineseWorth knowing
- rs10516809HERC5 · 88,499,935A;Acommon in complete genomicsTypical
- rs16996151FAM13A · 89,057,649C;Ccommon in complete genomicsTypical
- rs7668883LOC105377329 · 89,597,881A;Acommon genotypeTypical
- rs356219LOC105377329 · 89,716,450G;G1.6x increased risk for Parkinson's diseaseMinor
- rs11931074LOC105377329 · 89,718,364G;GNo summary available.Typical
- rs356220LOC105377329 · 89,720,189T;Tincreased risk of Parkinson's DiseaseMinor
- rs356165SNCA · 89,725,735G;Gcommon in clinvarTypical
- rs356168SNCA · 89,753,280A;Aslight decrease in risk for Parkinson's diseaseWorth knowing
- rs2736990SNCA · 89,757,390G;GSlightly increased risk of developing Parkinson's DiseaseWorth knowing
- rs3775442SNCA · 89,794,080C;Ccommon genotypeTypical
- rs104893877SNCA · 89,828,149C;TParkinson's disease mutation, adult-onsetVery important
- rs653219789,876,150G;GIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs966845PDLIM5 · 94,618,116A;Acommon in complete genomicsTypical
- rs13107595PDLIM5 · 94,657,437A;Acommon in complete genomicsTypical
- rs469958794,694,618A;ANo summary available.Typical
- rs1002762894,722,806T;Tcommon genotypeTypical
- rs1434536BMPR1B · 95,154,814T;T1.94x increased breast cancer riskWorth knowing
- rs11097457BMPR1B · 95,155,662A;Acommon in clinvarTypical
- rs12643654UNC5C · 95,238,666A;Acommon in complete genomicsTypical
- rs6827292ADH5 · 99,071,843T;Tcommon in complete genomicsTypical
- rs6819724LOC100507053 · 99,107,300A;Acommon in complete genomicsTypical
- rs3805322ADH4 · 99,135,847A;Acommon in complete genomicsTypical
- rs1800759ADH4 · 99,144,358T;Tincreased risk for alcohol or drug dependence; increased agreeableness (?)Typical
- rs17028615LOC100507053 · 99,150,767A;Acommon genotypeTypical
- rs2066702ADH1B · 99,307,860G;GcommonTypical
- rs17028834ADH1B · 99,311,443T;Tcommon in complete genomicsTypical
- rs6413413ADH1B · 99,318,127A;Acommon in complete genomicsTypical
- rs1229984ADH1B · 99,318,162T;T0.56x decreased risk of oral/throat cancersWorth knowing
- rs17856968ADH1B · 99,318,162T;TNo summary available.Typical
- rs178989199,329,262C;Ccommon on affy axiom dataTypical
- rs283411ADH1C · 99,344,800C;Ccommon in complete genomicsTypical
- rs283413ADH1C · 99,347,033A;A3x higher risk for PDWorth knowing
- rs3737482ADH7 · 99,428,309T;Tcommon in complete genomicsTypical
- rs1573496ADH7 · 99,428,512C;CnormalTypical
- rs2306986MTTP · 99,583,418G;Gcommon in clinvarTypical
- rs3816873MTTP · 99,583,507C;Creduced risk of type-2 diabetesWorth knowing
- rs3792683MTTP · 99,589,746A;Acommon in clinvarTypical
- rs2306985MTTP · 99,594,865C;Ccommon in clinvarTypical
- rs17029215MTTP · 99,600,648A;Acommon in complete genomicsTypical
- rs1405687101,010,669G;Gcommon in complete genomicsTypical
- rs2659546PPP3CA · 101,116,562C;Ccommon in complete genomicsTypical
- rs7700191101,668,126G;GNo summary available.Typical
- rs10516487BANK1 · 101,829,919A;Aslightly higher risk for lupusMinor
- rs35518360102,225,733A;TLikely miscall in 23andMe data; otherwise, slightly lower schizophrenia risk perhapsMinor
- rs13107325SLC39A8 · 102,267,552C;CNo summary available.Typical
- rs1585215NFKB1 · 102,523,317C;C3.5x increased risk for Hodgkin lymphomaWorth knowing
- rs13117745NFKB1 · 102,557,546T;TIncreased rectal cancer risk (1.22 - 1.66)Typical
- rs4648022NFKB1 · 102,575,280T;T0.47x reduced risk for NHLMinor
- rs2866413MANBA · 102,635,920A;GNo summary available.Typical
- rs227368MANBA · 102,690,688A;GNo summary available.Typical
- rs223469LOC102723704 · 102,778,621C;Ccommon in complete genomicsTypical
- rs7669317105,536,173T;Tcommon in complete genomicsTypical
- rs11727189INTS12 · 105,697,983G;GNo summary available.Typical
- rs10516526GSTCD · 105,767,747A;Acommon on affy axiom dataTypical
- rs17331332LOC101929558 · 105,886,950G;Gcommon genotypeTypical
- rs7680468107,383,042G;Gcommon genotypeTypical
- rs4956145HADH · 108,009,883C;CNo summary available.Typical
- rs221347HADH · 108,034,466T;Tcommon in clinvarTypical
- rs4698775MCUB · 109,669,323G;Gcommon in clinvarTypical
- rs141853578CFI · 109,764,664C;TPossibly: somewhat higher risk for age-related macular degenerationImportant
- rs4444903EGF · 109,912,954G;G3.5x risk of hep-cancer in cirrhosis patients; higher glioma risk; 3x higher gallbladder cancer risk in femalesWorth knowing
- rs11568943EGF · 109,961,965G;Gcommon in clinvarTypical
- rs11568995EGF · 109,976,429G;Gcommon genotypeTypical
- rs2237051EGF · 109,980,042G;Gcommon in clinvarTypical
- rs11569017EGF · 109,980,955A;Acommon in clinvarTypical
- rs4698803EGF · 109,993,271A;Acommon in clinvarTypical
- rs6533526PITX2 · 110,617,671G;Gcommon in clinvarTypical
- rs6817105110,784,612T;Tcommon/normalTypical
- rs17042171110,787,131C;Ccommon in complete genomicsTypical
- rs2200733LOC729065 · 110,789,013C;T1.4x increased risk of Atrial Fibrillation and ischemic stroke.Important
- rs4611994110,789,885T;Tcommon in complete genomicsTypical
- rs10033464110,799,605G;T1.28x increased risk of Atrial Fibrillation and cardioembolic stroke.Important
- rs17570669110,815,726A;Acommon in complete genomicsTypical
- rs3853445110,840,331T;Tcommon/normalTypical
- rs10034228111,690,594C;CNo summary available.Typical
- rs17589290112,002,081C;Ccommon in complete genomicsTypical
- rs4148254UGT8 · 114,623,557C;CNo summary available.Typical
- rs12510781114,719,425A;Acommon genotypeTypical
- rs13144478115,275,150A;Acommon in complete genomicsTypical
- rs1799883FABP2 · 119,320,747T;TTwo copies of the Thr allele in the FABP2 is associated with significantly increased sensitivity to saturated fats. Also contributes to increased refined carb sensitivity.Typical
- rs7659604121,744,359C;C1.1x risk of type II diabetesTypical
- rs4374642KIAA1109 · 122,179,956T;Tcommon in complete genomicsTypical
- rs13151961KIAA1109 · 122,194,347A;Acommon on affy axiom dataTypical
- rs17388568ADAD1 · 122,408,207A;A1.6x risk of type-1 diabetesTypical
- rs11732095ADAD1 · 122,427,190A;ANo summary available.Typical
- rs2069779IL2 · 122,452,742G;Gcommon in complete genomicsTypical
- rs6822844122,588,266G;Gcommon on affy axiom dataTypical
- rs4833837IL21 · 122,615,808G;Gcommon in clinvarTypical
- rs309375122,760,001C;CSmaller mosquito bitesMinor
- rs308393FGF2 · 122,825,464A;Acommon in complete genomicsTypical
- rs308395FGF2 · 122,825,787C;Ccommon in complete genomicsTypical
- rs7683093NUDT6 · 122,896,930C;CNo summary available.Typical
- rs6820411SPATA5 · 122,924,114C;CNo summary available.Typical
- rs1425419123,644,809C;Ccommon in complete genomicsTypical
- rs1986655125,072,347A;Acommon in complete genomicsTypical
- rs1039808FAT4 · 125,318,831C;Ccommon in clinvarTypical
- rs12508222FAT4 · 125,449,492G;Gcommon in clinvarTypical
- rs1567047FAT4 · 125,451,587G;Gcommon in clinvarTypical
- rs1014867FAT4 · 125,491,736C;Ccommon in clinvarTypical
- rs1443170LOC102724210 · 127,399,753T;Tcommon genotypeTypical
- rs10026364LOC105377436 · 134,601,585C;Ccommon in complete genomicsTypical
- rs2404646135,165,126C;Ccommon in complete genomicsTypical
- rs2313132137,771,096A;Acommon on affy axiom dataTypical
- rs1509269137,832,570C;Ccommon in complete genomicsTypical
- rs6847679137,841,472T;Tcommon in complete genomicsTypical
- rs2313982137,866,906G;Gcommon in complete genomicsTypical
- rs4956302141,543,569A;Acommon in complete genomicsTypical
- rs10519612IL15 · 141,732,548A;Acommon in complete genomicsTypical
- rs10519613IL15 · 141,732,931C;Ccommon in complete genomicsTypical
- rs35964658141,758,435A;Acommon in complete genomicsTypical
- rs17007695141,788,570T;Tcommon in complete genomicsTypical
- rs7683365GYPB · 143,999,443A;AMNS blood group S/S status predictedMinor
- rs1828591LOC105377462 · 144,559,628G;GReduced risk (0.54x) for chronic pulmonary obstructive disease (COPD)Worth knowing
- rs13149290ZNF827 · 145,829,814C;CSlightly increased risk of developing prostate cancerMinor
- rs5335EDNRA · 147,542,688C;Cnormal riskTypical
- rs7658486ARHGAP10 · 147,963,038C;Ccommon genotypeTypical
- rs5534NR3C2 · 148,079,934T;Tcommon in clinvarTypical
- rs11725509NR3C2 · 148,390,576A;ANo summary available.Typical
- rs5522NR3C2 · 148,436,323T;Tcommon on affy axiom dataTypical
- rs2070951NR3C2 · 148,436,862G;Gcommon in clinvarTypical
- rs360929151,986,548G;GNo summary available.Typical
- rs6842544FBXW7 · 152,411,407T;Tcommon in complete genomicsTypical
- rs6817112TRIM2 · 153,159,661C;Ccommon in complete genomicsTypical
- rs893629TLR2 · 153,683,816G;Gcommon genotypeTypical
- rs4696480TLR2 · 153,685,974A;Tpreterm birthMinor
- rs3804100TLR2 · 153,704,257C;Csomwhat increased risk for type-1 diabetes and allergic asthmaTypical
- rs5743708TLR2 · 153,705,165A;A6x increased risk of tuberculosisImportant
- rs902464DCHS2 · 154,394,970C;Ccommon genotypeTypical
- rs17031671DCHS2 · 154,468,095T;Tcommon genotypeTypical
- rs1800787FGB · 154,562,863T;TNo summary available.Typical
- rs6056FGB · 154,567,669C;Ccommon in clinvarTypical
- rs6054FGB · 154,568,456C;Ccommon in complete genomicsTypical
- rs4681FGB · 154,569,680C;Ccommon in clinvarTypical
- rs4220FGB · 154,570,607G;Gcommon in clinvarTypical
- rs1044291FGB · 154,572,200C;Ccommon in clinvarTypical
- rs2070022FGA · 154,583,796G;Gcommon in complete genomicsTypical
- rs10050257154,594,243T;Tcommon in complete genomicsTypical
- rs2066865FGG · 154,604,124G;Gcommon in clinvarTypical
- rs6063FGG · 154,609,725T;TNo summary available.Worth knowing
- rs17376826NPY2R · 155,209,796C;CNo summary available.Typical
- rs11559290ETFDH · 158,680,524C;Ccommon in clinvarTypical
- rs17291045160,585,745C;Ccommon on affy axiom dataTypical
- rs4470583161,329,780G;Gcommon in complete genomicsTypical
- rs17638464FSTL5 · 161,681,057G;Gcommon on affy axiom dataTypical
- rs4440177162,321,901A;ANo summary available.Typical
- rs10033119NPY1R · 163,324,702A;Acommon in complete genomicsTypical
- rs6837793NPY1R · 163,335,583A;AnormalTypical
- rs3792615MARCH1 · 163,611,649T;Tcommon in complete genomicsTypical
- rs6829588MARCH1 · 164,300,819G;Gcommon in complete genomicsTypical
- rs6812849TLL1 · 165,951,384C;Ccommon genotypeTypical
- rs13111850167,343,098T;TNo summary available.Typical
- rs17054392PALLD · 168,609,107T;Tcommon in complete genomicsTypical
- rs7439293PALLD · 168,756,335A;Aincreased risk of coronary heart disease; better response to statinsTypical
- rs1071738CBR4 · 168,928,238C;Ccommon in clinvarTypical
- rs4692788170,056,852C;CNo summary available.Typical
- rs8752HPGD · 174,491,326C;Ccommon in clinvarTypical
- rs17697305LOC105377555 · 176,685,497T;TNo summary available.Typical
- rs6838834VEGFC · 176,732,444C;Ccommon in complete genomicsTypical
- rs1983132LOC105377557 · 177,298,634C;T2 - 3x higher prostate cancer risk if routinely exposed to the pesticide fonofosImportant
- rs2228119AGA · 177,438,806G;Gcommon in clinvarTypical
- rs17746001179,734,472C;Ccommon genotypeTypical
- rs17090640179,746,494G;Gcommon genotypeTypical
- rs17074636183,356,978T;Tcommon genotypeTypical
- rs11132186183,517,570T;T0.5x decreased risk for bladder cancerWorth knowing
- rs3775572IRF2 · 184,448,298A;Acommon genotypeTypical
- rs5743311TLR3 · 186,079,010G;Gcommon in complete genomicsTypical
- rs5743315TLR3 · 186,079,262C;Ccommon in complete genomicsTypical
- rs3775291TLR3 · 186,082,920T;T0.44x decreased risk for dry age related macular degenerationWorth knowing
- rs1055138FLJ38576 · 186,191,887G;Glikely to be benignTypical
- rs13146272CYP4V2 · 186,199,057C;Ccommon in clinvarTypical
- rs3733403F11 · 186,265,981C;Ccommon in clinvarTypical
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.