ClinVar Miner

List of variants in gene KCNH2 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 45
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HGVS dbSNP
NM_000238.3(KCNH2):c.1067G>A (p.Arg356His) rs730880118
NM_000238.3(KCNH2):c.1189C>T (p.Arg397Cys) rs1060500663
NM_000238.3(KCNH2):c.1226T>A (p.Val409Glu) rs794728367
NM_000238.3(KCNH2):c.1291T>C (p.Phe431Leu) rs1554426244
NM_000238.3(KCNH2):c.1471G>A (p.Val491Ile) rs374376640
NM_000238.3(KCNH2):c.1525G>A (p.Asp509Asn) rs370637245
NM_000238.3(KCNH2):c.1603G>A (p.Val535Met) rs375872367
NM_000238.3(KCNH2):c.1693G>T (p.Ala565Ser) rs199473518
NM_000238.3(KCNH2):c.1805T>C (p.Leu602Pro) rs876661348
NM_000238.3(KCNH2):c.2144C>T (p.Ala715Val) rs780656919
NM_000238.3(KCNH2):c.2145+3G>A rs1378166842
NM_000238.3(KCNH2):c.215C>A (p.Pro72Gln) rs199473421
NM_000238.3(KCNH2):c.2296G>A (p.Gly766Arg) rs1057524377
NM_000238.3(KCNH2):c.2343C>G (p.Phe781Leu) rs886039215
NM_000238.3(KCNH2):c.2366T>C (p.Ile789Thr) rs794728388
NM_000238.3(KCNH2):c.2371C>T (p.Arg791Trp) rs138498207
NM_000238.3(KCNH2):c.2387T>G (p.Val796Gly) rs1554425163
NM_000238.3(KCNH2):c.2525T>C (p.Leu842Pro) rs1554424818
NM_000238.3(KCNH2):c.2616C>A (p.Pro872=) rs374296728
NM_000238.3(KCNH2):c.2674C>T (p.Arg892Cys) rs201627778
NM_000238.3(KCNH2):c.2696C>G (p.Thr899Arg) rs1480554629
NM_000238.3(KCNH2):c.2707G>A (p.Gly903Arg) rs199473669
NM_000238.3(KCNH2):c.2729C>T (p.Pro910Leu) rs199473436
NM_000238.3(KCNH2):c.2738C>T (p.Ala913Val) rs77331749
NM_000238.3(KCNH2):c.2759G>A (p.Arg920Gln) rs199473670
NM_000238.3(KCNH2):c.2770G>T (p.Gly924Trp) rs794728397
NM_000238.3(KCNH2):c.2771G>A (p.Gly924Glu) rs199473009
NM_000238.3(KCNH2):c.2771G>C (p.Gly924Ala) rs199473009
NM_000238.3(KCNH2):c.2860C>T (p.Arg954Cys) rs141401803
NM_000238.3(KCNH2):c.2941A>G (p.Ser981Gly) rs76649554
NM_000238.3(KCNH2):c.298C>G (p.Arg100Gly) rs121912515
NM_000238.3(KCNH2):c.3164G>A (p.Arg1055Gln) rs41307270
NM_000238.3(KCNH2):c.3203A>G (p.Gln1068Arg) rs151031345
NM_000238.3(KCNH2):c.3251C>T (p.Pro1084Leu) rs762510312
NM_000238.3(KCNH2):c.3289G>A (p.Val1097Ile) rs199473030
NM_000238.3(KCNH2):c.3436A>T (p.Thr1146Ser) rs778879572
NM_000238.3(KCNH2):c.374T>G (p.Phe125Cys) rs199473499
NM_000238.3(KCNH2):c.473-5C>T rs1181633993
NM_000238.3(KCNH2):c.526C>T (p.Arg176Trp) rs36210422
NM_000238.3(KCNH2):c.607G>A (p.Ala203Thr) rs199472868
NM_000238.3(KCNH2):c.695G>T (p.Arg232Leu) rs886039160
NM_000238.3(KCNH2):c.865G>A (p.Glu289Lys) rs199472880
NM_000238.3(KCNH2):c.916+3G>A rs1554427591
NM_000238.3(KCNH2):c.980A>G (p.Tyr327Cys) rs886039013
NM_000238.3(KCNH2):c.982C>T (p.Arg328Cys) rs199473505

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