Chromosome 19
276 well-documented SNPs on chromosome 19, in order of position (GRCh38).
- rs11085226PTBP1 · 799,770A;Acommon genotypeTypical
- rs137854448ELANE · 855,613C;TMaybe: Severe congenital neutropenia, type 1, autosomal dominant; see discussionVery important
- rs3764650ABCA7 · 1,046,521G;GLate onset?Typical
- rs115550680ABCA7 · 1,050,421G;GIncreased risk (~2.2x?) of Alzheimer's, observed for African-AmericansWorth knowing
- rs3752246ABCA7 · 1,056,493C;Ccommon on affy axiom dataTypical
- rs4147918ABCA7 · 1,058,177A;Acommon genotypeTypical
- rs4921POLR2E · 1,093,980C;Ccommon in complete genomicsTypical
- rs713041GPX4 · 1,106,616C;CnormalTypical
- rs3764640STK11 · 1,207,239G;Gcommon in clinvarTypical
- rs9282860STK11 · 1,221,162T;Tslightly increased risk for multiple sclerosis in femalesWorth knowing
- rs121913322STK11 · 1,221,320C;TSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs59912467STK11 · 1,223,126C;Gsomewhat possible association with Peutz-Jeghers syndromeWorth knowing
- rs1142530NDUFS7 · 1,388,539C;Ccommon in clinvarTypical
- rs7250872ATP8B3 · 1,811,604T;TIncreased risk of developing bipolar disorderWorth knowing
- rs25673AP3D1 · 2,109,158T;Tcommon on affy axiom dataTypical
- rs10407022AMH · 2,249,478T;TNo summary available.Typical
- rs4523TBXA2R · 3,595,796A;Acommon in clinvarTypical
- rs10412199ATCAY · 3,927,773G;Gcommon in clinvarTypical
- rs107251SIRT6 · 4,176,088C;Ccommon in complete genomicsTypical
- rs2292151TICAM1 · 4,816,707G;Gcommon in clinvarTypical
- rs1978237PTPRS · 5,209,630C;C>1.59x risk of Type 2 diabetesMinor
- rs1143699PTPRS · 5,210,751G;GIn men, 2.19x risk of type 2 diabetesWorth knowing
- rs4807015PTPRS · 5,231,124C;C>1.74x risk of type 2 diabetesMinor
- rs3760776FUT6 · 5,839,735G;Gcommon in complete genomicsTypical
- rs16994592CD70 · 6,586,487T;Tcommon in complete genomicsTypical
- rs344560TNFSF14 · 6,665,009C;Ccommon in complete genomicsTypical
- rs2291667TNFSF14 · 6,669,975G;Gcommon in complete genomicsTypical
- rs11569562C3 · 6,678,742G;Gincreased risk for adult asthmaTypical
- rs2277984C3 · 6,679,500C;Ccommon in clinvarTypical
- rs7951C3 · 6,681,980G;Gcommon in clinvarTypical
- rs2241394C3 · 6,685,219G;Gcommon in complete genomicsTypical
- rs11569536C3 · 6,686,078G;Gcommon genotypeTypical
- rs2230205C3 · 6,709,693C;Ccommon in clinvarTypical
- rs2230201C3 · 6,713,280C;C>1.4x risk of lupusWorth knowing
- rs2230199C3 · 6,718,376C;G1.6x+ risk of ARMDWorth knowing
- rs1051690INSR · 7,116,952T;Tcommon in clinvarTypical
- rs1799817INSR · 7,125,286G;Gcommon in clinvarTypical
- rs2059806INSR · 7,166,365C;Ccommon in clinvarTypical
- rs6603109ARHGEF18 · 7,359,642A;Acommon in complete genomicsTypical
- rs104886461LOC105372261 · 7,526,759G;GMucolipidosis type IVVery important
- rs2303116STXBP2 · 7,641,770C;Ccommon in clinvarTypical
- rs3219175RETN · 7,668,969G;Gcommon in complete genomicsTypical
- rs4804803CD209 · 7,747,847A;ANo summary available.Typical
- rs558718EVI5L · 7,844,997A;Acommon in complete genomicsTypical
- rs9426CD320 · 8,302,274C;Ccommon in complete genomicsTypical
- rs2336573CD320 · 8,302,825C;Ccommon in complete genomicsTypical
- rs116843064ANGPTL4 · 8,364,439G;Gcommon on affy axiom dataTypical
- rs2967605RAB11B · 8,404,854C;CNo summary available.Typical
- rs7255721ADAMTS10 · 8,605,046G;Gcommon in clinvarTypical
- rs5020278OR7D4 · 9,214,440A;A"sweet" smellerTypical
- rs2233682PIN1 · 9,838,476G;Gcommon in complete genomicsTypical
- rs15723ANGPTL6 · 10,092,495A;ANo summary available.Typical
- rs8109578ANGPTL6 · 10,102,478G;Gcommon on affy axiom dataTypical
- rs2305795EIF3G · 10,115,376A;A1.64x higher risk of narcolepsy compared to (G;G) genotypeWorth knowing
- rs2228611DNMT1 · 10,156,401T;Tcommon in clinvarTypical
- rs16999358DNMT1 · 10,162,679G;Gcommon in clinvarTypical
- rs2228612DNMT1 · 10,162,696T;Tcommon in clinvarTypical
- rs16999593DNMT1 · 10,180,505T;Tcommon in complete genomicsTypical
- rs5490LOC105372272 · 10,271,151A;Acommon in complete genomicsTypical
- rs5491LOC105372272 · 10,274,864A;Acommon in complete genomicsTypical
- rs1799969LOC105372272 · 10,284,116A;Aslightly higher breast cancer riskTypical
- rs5496LOC105372272 · 10,284,771G;GAncestral GenotypeTypical
- rs5498LOC105372272 · 10,285,007A;AnormalTypical
- rs34536443TYK2 · 10,352,442C;CMuch higher (90 fold) risk of developing tuberculosis if exposed to TB bacteriumVery important
- rs12720356TYK2 · 10,359,299A;Acommon on affy axiom dataTypical
- rs280519TYK2 · 10,362,257A;Acommon in clinvarTypical
- rs2304256TYK2 · 10,364,976C;C1.6x increased risk for SLETypical
- rs280523TYK2 · 10,366,530G;Gcommon in clinvarTypical
- rs280500TYK2 · 10,379,726A;Acommon in clinvarTypical
- rs2288904SLC44A2 · 10,631,494C;CNo summary available.Typical
- rs892086DNM2 · 10,727,001C;TNo summary available.Typical
- rs11671653DNM2 · 10,727,810G;Gcommon in complete genomicsTypical
- rs11669133SMARCA4 · 10,981,463G;Gcommon in complete genomicsTypical
- rs1166847711,084,354A;ANo summary available.Typical
- rs6511720LDLR · 11,091,630G;TSlightly lower odds of developing CHD.Worth knowing
- rs2228671LDLR · 11,100,236A;CFamilial HypercholesterolemiaVery important
- rs201102461LDLR · 11,105,250A;GFamilial Hypercholesterolemia (possible but uncertain)Very important
- rs121908034LDLR · 11,105,470A;CFamilial HypercholesterolemiaVery important
- rs121908029LDLR · 11,105,588A;GFamilial HypercholesterolemiaVery important
- rs11669576LDLR · 11,111,624G;Gcommon in clinvarTypical
- rs121908043LDLR · 11,113,307A;CFamilial HypercholesterolemiaVery important
- rs1003723LDLR · 11,113,505C;Ccommon in clinvarTypical
- rs5930LDLR · 11,113,589A;Acommon in clinvarTypical
- rs5929LDLR · 11,116,124C;Ccommon in clinvarTypical
- rs688LDLR · 11,116,926C;Cnormal riskTypical
- rs2569548LDLR · 11,120,435C;TFamilial HypercholesterolemiaVery important
- rs5927LDLR · 11,123,265A;Acommon in clinvarTypical
- rs137853964LDLR · 11,129,602G;TFamilial HypercholesterolemiaVery important
- rs6413503LDLR · 11,131,228G;Gcommon in complete genomicsTypical
- rs1433099LDLR · 11,131,982T;Tcommon in clinvarTypical
- rs121918116EPOR · 11,378,194C;Tbenign erythrocytosis, resulting in more red blood cellsImportant
- rs11557488PRKCSH · 11,447,460G;Gcommon in clinvarTypical
- rs11880637CNN1 · 11,544,195A;Acommon genotypeTypical
- rs7253363LOC101928434 · 11,571,680G;Gcommon on affy axiom dataTypical
- rs3745672ZNF433 · 12,035,555T;Tcommon in complete genomicsTypical
- rs17638629LOC105372275 · 12,114,557T;Tcommon in complete genomicsTypical
- rs10411619LOC105372279 · 12,641,611T;Tcommon genotypeTypical
- rs11085825GCDH · 12,896,644C;Tmost likely benign polymorphismMinor
- rs8012GCDH · 12,899,706A;Abenign allele wrt glutaric acidemiaTypical
- rs9384GCDH · 12,899,829G;Gcommon in clinvarTypical
- rs12327666RLN3 · 14,029,109G;GNo summary available.Typical
- rs452868414,240,762C;Ccommon in complete genomicsTypical
- rs3745459PTGER1 · 14,473,505G;Gcommon in complete genomicsTypical
- rs1044009NOTCH3 · 15,160,960G;Gcommon in clinvarTypical
- rs3815188NOTCH3 · 15,192,414G;Gcommon in clinvarTypical
- rs3764563CYP4F8 · 15,613,392G;Gcommon in complete genomicsTypical
- rs3093200CYP4F2 · 15,878,779G;Gcommon on affy axiom dataTypical
- rs2108622CYP4F2 · 15,879,621C;Clower warfarin dosingWorth knowing
- rs8109288TPM4 · 16,074,749G;Gcommon in complete genomicsTypical
- rs142951029CALR3 · 16,490,519C;Tlikely to be benignMinor
- rs2305767MYO9B · 17,183,487T;Tcommon/normalTypical
- rs12608932UNC13A · 17,641,880C;CSmall increase in ALS risk; better lithium response in ALS patientsWorth knowing
- rs36686B3GNT3 · 17,811,986A;Acommon in complete genomicsTypical
- rs3213409JAK3 · 17,834,887C;Ccommon in complete genomicsTypical
- rs3212752JAK3 · 17,837,923T;Tcommon in clinvarTypical
- rs3212723JAK3 · 17,843,406G;Gcommon in clinvarTypical
- rs4808708SLC5A5 · 17,890,877G;Gcommon in clinvarTypical
- rs12327843SLC5A5 · 17,894,103T;Tcommon in clinvarTypical
- rs375947IL12RB1 · 18,069,641A;Acommon in clinvarTypical
- rs11575934IL12RB1 · 18,075,808T;Tcommon in clinvarTypical
- rs436857IL12RB1 · 18,086,825G;Gcommon in clinvarTypical
- rs393548IL12RB1 · 18,086,934T;Tcommon in clinvarTypical
- rs3764628KLHL26 · 18,636,795G;Gcommon in complete genomicsTypical
- rs28936368COMP · 18,783,129G;Gcommon in clinvarTypical
- rs2228603NCAN · 19,219,115T;Thepatic steatosisImportant
- rs1064395NCAN · 19,250,926A;AHaving the A allele at this SNP makes your risk for developing bipolar disorder or schizophrenia higher.Worth knowing
- rs58542926TM6SF2 · 19,268,740C;TComplex; slightly lower risk of heart attacks, yet slightly higher risk for diabetes and NAFLDWorth knowing
- rs10401969SUGP1 · 19,296,909T;Tcommon in complete genomicsTypical
- rs16996148CILP2 · 19,547,663G;Gcommon in complete genomicsTypical
- rs1721652519,551,411C;Ccommon in complete genomicsTypical
- rs12610185PBX4 · 19,610,913G;Gcommon genotypeTypical
- rs2304130ZNF101 · 19,678,719A;Acommon in complete genomicsTypical
- rs10411195ZNF93 · 19,925,367T;Tcommon in complete genomicsTypical
- rs725058129,573,489G;G1.4x riskWorth knowing
- rs997669CCNE1 · 29,813,576C;CVery slightly increased (1.18x) increased breast cancer riskMinor
- rs3218038CCNE1 · 29,814,988G;Gcommon genotypeTypical
- rs1245989731,105,872G;GNo summary available.Typical
- rs11880316LOC107985311 · 31,420,223C;Ccommon genotypeTypical
- rs17692896ANKRD27 · 32,598,525G;GNo summary available.Typical
- rs1007160SLC7A9 · 32,862,155G;Gcommon in clinvarTypical
- rs12150889SLC7A9 · 32,864,149A;Acommon in clinvarTypical
- rs10411210RHPN2 · 33,041,394T;T1.15x increased risk of colorectal cancerWorth knowing
- rs1050026433,259,408G;Gcommon in complete genomicsTypical
- rs4805924CHST8 · 33,677,367C;Ccommon in complete genomicsTypical
- rs2301600MAG · 35,295,965C;Ccommon in clinvarTypical
- rs892055RASGRP4 · 38,422,124A;Acommon in complete genomicsTypical
- rs118192161RYR1 · 38,444,211C;Tsusceptibility to malignant hyperthermiaImportant
- rs118192172RYR1 · 38,457,545C;Tsusceptibility to malignant hyperthermiaImportant
- rs10500279RYR1 · 38,544,428G;Gcommon in complete genomicsTypical
- rs11881222IL28B · 39,244,283A;Acommon in clinvarTypical
- rs12979860IFNL4 · 39,248,147T;T~20-25% of such hepatitis C patients respond to treatmentImportant
- rs809991739,252,525G;Glower odds of responding to PEG-IFNalpha/RBV treatmentImportant
- rs30461IFNL1 · 39,298,475A;Acommon in complete genomicsTypical
- rs1110627DLL3 · 39,504,071T;Tcommon in clinvarTypical
- rs17608CLC · 39,735,006A;ANo summary available.Typical
- rs367643250DYRK1B · 39,830,443A;Gcausative for obesity, coronary artery disease, type-2 diabetes?Very important
- rs11673492COQ8B · 40,714,624C;Ccommon in clinvarTypical
- rs28493229COQ8B · 40,718,299G;GNo summary available.Typical
- rs5031017CYP2A6 · 40,843,845A;ATwo copies of CYP2A6*5 non-functioning variant; impaired nicotine metabolismWorth knowing
- rs28399454CYP2A6 · 40,845,362C;Ccommon in complete genomicsTypical
- rs4997557CYP2A6 · 40,846,048G;Gcommon in complete genomicsTypical
- rs1801272CYP2A6 · 40,848,628T;TReduced CYP2A6 metabolism; impaired nicotine metabolism?Worth knowing
- rs8192709CYP2B6 · 40,991,369C;Ccommon in complete genomicsTypical
- rs3745274CYP2B6 · 41,006,936T;TIf efavirenz is ever prescribed for you, lower doses may be advisableWorth knowing
- rs2279343CYP2B6 · 41,009,358G;GLower doses of efavirenz for treating HIV may be recommendedWorth knowing
- rs2279345CYP2B6 · 41,009,797T;Tcommon in clinvarTypical
- rs28399499CYP2B6 · 41,012,316T;Tcommon in complete genomicsTypical
- rs7249222AXL · 41,237,956G;Gcommon in complete genomicsTypical
- rs11881940HNRNPUL1 · 41,302,527A;Anormal formTypical
- rs8179181TGFB1 · 41,332,301G;Gcommon in clinvarTypical
- rs8110090TGFB1 · 41,339,967A;Acommon in complete genomicsTypical
- rs1800472TGFB1 · 41,341,955G;Gcommon on affy axiom dataTypical
- rs4803455TGFB1 · 41,345,604C;Ccommon in clinvarTypical
- rs2241715TGFB1 · 41,350,981A;Acommon in clinvarTypical
- rs1800471TGFB1 · 41,352,971C;Ccommon in clinvarTypical
- rs1800470TGFB1 · 41,353,016A;GNo summary available.Typical
- rs1982073TGFB1 · 41,353,016G;Grisk genotype for several disordersTypical
- rs1800469TGFB1 · 41,354,391G;Glower TGF-β1 levels, higher risk for COPD?Minor
- rs2241714B9D2 · 41,363,487T;Tcommon in clinvarTypical
- rs11672691PCAT19 · 41,479,679G;G1.39x increased risk for PCSM in patients with prostate cancerWorth knowing
- rs887391PCAT19 · 41,479,716C;CLower prostate cancer risk?Minor
- rs10407503CEACAM5 · 41,717,515C;Ccommon in complete genomicsTypical
- rs7249230CEACAM5 · 41,717,688G;Gcommon on affy axiom dataTypical
- rs707746PSG2 · 43,071,794T;Tcommon in complete genomicsTypical
- rs25487XRCC1 · 43,551,574T;T0.7x lower risk for skin cancerWorth knowing
- rs25489XRCC1 · 43,552,260T;T4.68x higher risk for breast cancerTypical
- rs1799782XRCC1 · 43,553,422A;A1.4x increased risk for oral cancer among AsiansMinor
- rs2306801KCNN4 · 43,776,326A;ANo summary available.Typical
- rs670950KCNN4 · 43,777,410C;Ccommon in complete genomicsTypical
- rs1434579ZNF229 · 44,428,797C;Ccommon in complete genomicsTypical
- rs4803750BCL3 · 44,744,370A;ANo summary available.Typical
- rs1135062BCAM · 44,819,487A;AAu(a)/Au(a) genotype; basically, Au(a) homozygoteTypical
- rs6857NECTIN2 · 44,888,997C;Ccommon/normalTypical
- rs2075650TOMM40 · 44,892,362A;Gpossibly 2x higher Alzheimer's riskWorth knowing
- rs157582TOMM40 · 44,892,962T;TWeaker memory performanceWorth knowing
- rs440446APOE · 44,905,910C;CnormalTypical
- rs527236160APOE · 44,908,587G;Gcommon in clinvarTypical
- rs429358APOE · 44,908,684C;Cone of 2 snps relevant to classifying APOE genotypeMinor
- rs267606664APOE · 44,908,730A;GRare ApoE1 allele; clinical significance unclearVery important
- rs121918393APOE · 44,908,756A;ATwo copies of ApoE3 Christchurch variant (apparently)Very important
- rs387906567APOE · 44,908,774C;TFamilial type 3 hyperlipoproteinemiaImportant
- rs769455APOE · 44,908,783C;Ccommon in clinvarTypical
- rs121918394APOE · 44,908,786A;GHyperlipoproteinemia, type IIIVery important
- rs7412APOE · 44,908,822C;Cpart of APOE4 genoset evaluationMinor
- rs199768005APOE · 44,909,057A;TMarked reduced risk of Alzheimer's DiseaseWorth knowing
- rs445925LOC100129500 · 44,912,383A;AAPOE E2/E2 most likely; lower Alzheimer's riskVery important
- rs12721054APOC1 · 44,919,330A;ANo summary available.Typical
- rs4420638APOC1 · 44,919,689G;G2x+ increased Alzheimer's risk, further genotyping suggested ; increased LDL cholesterolImportant
- rs5122APOC2 · 44,948,823G;Gcommon in clinvarTypical
- rs5126APOC2 · 44,949,172A;Acommon in clinvarTypical
- rs1041308944,952,331C;Csusceptibility to low HDL-cholesterolTypical
- rs13181ERCC2 · 45,351,661G;G>1.12x increased risk for cutaneous melanoma; possible increase in ovarian cancer riskWorth knowing
- rs238417ERCC2 · 45,353,210G;Gcommon in clinvarTypical
- rs3916840ERCC2 · 45,359,039G;Gcommon in complete genomicsTypical
- rs1799793ERCC2 · 45,364,001C;Ccommon in clinvarTypical
- rs238406ERCC2 · 45,365,051T;Tcommon in clinvarTypical
- rs2070830PPP1R13L · 45,386,392C;Ccommon in complete genomicsTypical
- rs3212989CD3EAP · 45,408,812A;Acommon in clinvarTypical
- rs3212986ERCC1 · 45,409,478C;Ccommon in clinvarTypical
- rs11615ERCC1 · 45,420,395A;Acommon in clinvarTypical
- rs1800437GIPR · 45,678,134C;CaverageTypical
- rs7245708QPCTL · 45,692,498A;Acommon genotypeTypical
- rs527221DMPK · 45,772,718G;Gcommon on affy axiom dataTypical
- rs8111071RSPH6A · 45,804,148A;AnormalTypical
- rs28937903FKRP · 46,756,814C;Ccommon in clinvarTypical
- rs11668878SLC1A5 · 46,765,116G;Gcommon on affy axiom dataTypical
- rs3810294BBC3 · 47,228,572C;Ccommon in complete genomicsTypical
- rs2547231SULT2A1 · 47,881,800C;CDecreased levels of some blood metabolitesWorth knowing
- rs263712547,898,636G;Gcommon on affy axiom dataTypical
- rs8110925PLA2G4C-AS1 · 48,060,175A;Acommon in complete genomicsTypical
- rs2307276PLA2G4C-AS1 · 48,061,950G;Gcommon in complete genomicsTypical
- rs20580LIG1 · 48,151,296G;Gcommon in clinvarTypical
- rs492602FUT2 · 48,703,160G;GHigher B12 levels in womenMinor
- rs1047781FUT2 · 48,703,374A;AABH blood group "Secretor" status if JapaneseTypical
- rs601338FUT2 · 48,703,417A;Aresistance to Norovirus infectionWorth knowing
- rs602662FUT2 · 48,703,728A;AHigher vitamin B12 levelsWorth knowing
- rs281379MAMSTR · 48,711,017G;GNo summary available.Typical
- rs2287921RASIP1 · 48,725,015C;Tcommon in complete genomicsTypical
- rs150074056FUT1 · 48,750,933A;APara-Bombay phenotype (blood transfusion consequences)Worth knowing
- rs838133FUT1 · 48,756,272A;ASweet Tooth; Higher odds of preferring candyMinor
- rs1800447LHB · 49,016,648A;Acommon in clinvarTypical
- rs2280401RPS11 · 49,496,752G;Gcommon in complete genomicsTypical
- rs3810265RPS9P4 · 49,720,009G;Gcommon in complete genomicsTypical
- rs810215049,727,070C;Ccommon genotypeTypical
- rs2017698MED25 · 49,834,979C;Ccommon in clinvarTypical
- rs648298MYH14 · 50,189,876T;TNo summary available.Typical
- rs1052471POLD1 · 50,406,437C;THigh risk of colorectal cancer; endometrial cancer risk also elevatedVery important
- rs3745516SPIB · 50,423,485A;AIncreased risk of developing primary biliary cirrhosisWorth knowing
- rs5515KLK1 · 50,820,420C;Ccommon in clinvarTypical
- rs17632542KLK3 · 50,858,501T;Tcommon in complete genomicsTypical
- rs2735839KLK3 · 50,861,367A;Ain prostrate cancer patients, this is statistically associated with a somewhat more aggressive cancerMinor
- rs7245858ZDHHC11B · 50,927,340A;ANo summary available.Typical
- rs3865444CD33 · 51,224,706A;Aslight reduction in risk for Alzheimer's diseaseMinor
- rs1041468951,293,045T;Tcommon genotypeTypical
- rs1130426ETFB · 51,347,036G;Gcommon in clinvarTypical
- rs1543922ZNF175 · 51,581,583C;Ccommon in complete genomicsTypical
- rs1042229FPR1 · 51,746,419A;Acommon in clinvarTypical
- rs5030878FPR1 · 51,746,963A;Acommon in clinvarTypical
- rs16984547ZNF665 · 53,178,789T;Tcommon in complete genomicsTypical
- rs13382089MIR521-2 · 53,716,600G;Gcommon in complete genomicsTypical
- rs2242245PRKCG · 53,900,547T;Tcommon genotypeTypical
- rs612529VSTM1 · 54,063,999A;Acommon/normalTypical
- rs7595TSEN34 · 54,193,224C;Ccommon in clinvarTypical
- rs2241524LILRA2 · 54,587,200G;GnormalTypical
- rs1671152GP6 · 55,014,977G;Gcommon in complete genomicsTypical
- rs2304167GP6 · 55,015,713C;Ccommon in clinvarTypical
- rs1654416GP6 · 55,018,667C;Ccommon in clinvarTypical
- rs1613662GP6 · 55,025,227A;Acommon in complete genomicsTypical
- rs104894729TNNI3 · 55,151,892C;TFamilial Hypertrophic CardiomyopathyVery important
- rs267607129TNNI3 · 55,151,912C;GFamilial Hypertrophic CardiomyopathyVery important
- rs121917761TNNI3 · 55,154,068T;TFamilial restrictive cardiomyopathy, type 1, as a possibilityVery important
- rs104894724TNNI3 · 55,154,146C;GFamilial Hypertrophic CardiomyopathyVery important
- rs77615401TNNI3 · 55,156,239A;AFamilial hypertrophic cardiomyopathy, type 7 (possibly)Very important
- rs17634917LOC105372465 · 55,754,298A;Acommon genotypeTypical
- rs204359955,939,683A;Acommon genotypeTypical
- rs260461ZNF544 · 58,259,517A;ANo summary available.Typical
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.