ClinVar Miner

List of variants in gene KCNH2 studied for Arrhythmia

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
Download table as spreadsheet
HGVS dbSNP
NM_000238.3(KCNH2):c.1035C>T (p.Gly345=)
NM_000238.3(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_000238.3(KCNH2):c.1071G>T (p.Glu357Asp)
NM_000238.3(KCNH2):c.1128+1784C>T rs371509270
NM_000238.3(KCNH2):c.1128+1803G>A
NM_000238.3(KCNH2):c.1128+1811G>A
NM_000238.3(KCNH2):c.1128+1852G>A rs780068180
NM_000238.3(KCNH2):c.1128+1861G>A
NM_000238.3(KCNH2):c.1189C>T (p.Arg397Cys) rs1060500663
NM_000238.3(KCNH2):c.1263G>A (p.Thr421=)
NM_000238.3(KCNH2):c.1320G>T (p.Pro440=) rs144926928
NM_000238.3(KCNH2):c.1332G>A (p.Glu444=) rs9770044
NM_000238.3(KCNH2):c.1467C>T (p.Ile489=) rs740952
NM_000238.3(KCNH2):c.1471G>A (p.Val491Ile) rs374376640
NM_000238.3(KCNH2):c.1528C>T (p.Leu510=) rs75648145
NM_000238.3(KCNH2):c.1539C>T (p.Phe513=) rs1805120
NM_000238.3(KCNH2):c.1558-5C>T rs114186001
NM_000238.3(KCNH2):c.1563C>T (p.Ile521=) rs143011005
NM_000238.3(KCNH2):c.157G>C (p.Gly53Arg) rs199472842
NM_000238.3(KCNH2):c.1582C>T (p.Arg528Trp) rs864622403
NM_000238.3(KCNH2):c.1641G>A (p.Ala547=) rs149902084
NM_000238.3(KCNH2):c.1692A>G (p.Leu564=) rs1805121
NM_000238.3(KCNH2):c.1800C>T (p.Ser600=) rs143518632
NM_000238.3(KCNH2):c.1809C>T (p.Gly603=) rs41314375
NM_000238.3(KCNH2):c.1887C>T (p.Asn629=)
NM_000238.3(KCNH2):c.1956T>C (p.Tyr652=) rs1137617
NM_000238.3(KCNH2):c.2127C>T (p.Asn709=) rs768572372
NM_000238.3(KCNH2):c.2131A>G (p.Ile711Val) rs199473532
NM_000238.3(KCNH2):c.227G>T (p.Arg76Leu)
NM_000238.3(KCNH2):c.2398+105delC rs546898924
NM_000238.3(KCNH2):c.2398+122T>C
NM_000238.3(KCNH2):c.2398+155C>A
NM_000238.3(KCNH2):c.2398+155C>T
NM_000238.3(KCNH2):c.2398+156G>A rs139247073
NM_000238.3(KCNH2):c.2398+178C>T rs41314366
NM_000238.3(KCNH2):c.2398+25G>T
NM_000238.3(KCNH2):c.2398+87C>T
NM_000238.3(KCNH2):c.2454G>A (p.Ser818=) rs72549418
NM_000238.3(KCNH2):c.2457C>T (p.Asn819=)
NM_000238.3(KCNH2):c.2566C>G (p.Leu856Val)
NM_000238.3(KCNH2):c.2616C>T (p.Pro872=) rs374296728
NM_000238.3(KCNH2):c.2617G>A (p.Gly873Ser) rs41314354
NM_000238.3(KCNH2):c.2660G>T (p.Arg887Leu)
NM_000238.3(KCNH2):c.2665T>G (p.Leu889Val) rs765427343
NM_000238.3(KCNH2):c.2685G>A (p.Thr895=)
NM_000238.3(KCNH2):c.2690A>C (p.Lys897Thr) rs1805123
NM_000238.3(KCNH2):c.2707G>A (p.Gly903Arg) rs199473669
NM_000238.3(KCNH2):c.2738C>T (p.Ala913Val) rs77331749
NM_000238.3(KCNH2):c.2739G>A (p.Ala913=) rs776097223
NM_000238.3(KCNH2):c.2758C>G (p.Arg920Gly) rs199473438
NM_000238.3(KCNH2):c.2768C>T (p.Pro923Leu)
NM_000238.3(KCNH2):c.2778G>A (p.Pro926=) rs898987242
NM_000238.3(KCNH2):c.278A>G (p.Lys93Arg) rs780197027
NM_000238.3(KCNH2):c.2823T>C (p.Ser941=)
NM_000238.3(KCNH2):c.2832G>C (p.Glu944Asp)
NM_000238.3(KCNH2):c.2861G>A (p.Arg954His) rs772977598
NM_000238.3(KCNH2):c.2932G>A (p.Glu978Lys) rs141117135
NM_000238.3(KCNH2):c.2941A>G (p.Ser981Gly) rs76649554
NM_000238.3(KCNH2):c.2948C>T (p.Thr983Ile) rs149955375
NM_000238.3(KCNH2):c.2966-4G>A
NM_000238.3(KCNH2):c.2967C>T (p.Gly989=)
NM_000238.3(KCNH2):c.300G>T (p.Arg100=)
NM_000238.3(KCNH2):c.3048C>T (p.Pro1016=)
NM_000238.3(KCNH2):c.3107G>A (p.Gly1036Asp) rs199473022
NM_000238.3(KCNH2):c.3109G>A (p.Asp1037Asn) rs199473023
NM_000238.3(KCNH2):c.3140G>A (p.Arg1047His)
NM_000238.3(KCNH2):c.3140G>T (p.Arg1047Leu) rs36210421
NM_000238.3(KCNH2):c.3162C>G (p.Thr1054=)
NM_000238.3(KCNH2):c.3211A>G (p.Met1071Val)
NM_000238.3(KCNH2):c.3224C>A (p.Pro1075Gln)
NM_000238.3(KCNH2):c.3229G>A (p.Ala1077Thr) rs201382073
NM_000238.3(KCNH2):c.3278C>T (p.Pro1093Leu) rs199473545
NM_000238.3(KCNH2):c.3301C>T (p.Pro1101Ser) rs1347039291
NM_000238.3(KCNH2):c.3321G>A (p.Ser1107=) rs189457419
NM_000238.3(KCNH2):c.3399A>G (p.Thr1133=)
NM_000238.3(KCNH2):c.342C>T (p.Pro114=) rs532959204
NM_000238.3(KCNH2):c.3436A>T (p.Thr1146Ser) rs778879572
NM_000238.3(KCNH2):c.3453C>A (p.His1151Gln)
NM_000238.3(KCNH2):c.3457C>T (p.His1153Tyr) rs199473035
NM_000238.3(KCNH2):c.442C>T (p.Arg148Trp) rs139544114
NM_000238.3(KCNH2):c.455C>G (p.Thr152Ser) rs794728354
NM_000238.3(KCNH2):c.460T>C (p.Trp154Arg)
NM_000238.3(KCNH2):c.51C>G (p.Thr17=) rs144338227
NM_000238.3(KCNH2):c.77-5C>A rs72549419
NM_000238.3(KCNH2):c.77-5C>G rs72549419
NM_000238.3(KCNH2):c.918G>A (p.Gly306=)
NM_000238.3(KCNH2):c.957C>T (p.Thr319=)
NM_000238.3(KCNH2):c.979T>C (p.Tyr327His)
NM_001204798.1(KCNH2):c.78C>T (p.Ala26=) rs200324802
NM_172057.2(KCNH2):c.2311-9_2311-8del rs41313749

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.