ClinVar Miner

List of variants in gene KCNH2 reported as benign

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Total variants: 76
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HGVS dbSNP
NC_000007.14:g.150952172del
NM_000238.3(KCNH2):c.-13-7_-12del rs754605400
NM_000238.3(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_000238.3(KCNH2):c.1128+1784C>T rs371509270
NM_000238.3(KCNH2):c.1128+2093G>C
NM_000238.3(KCNH2):c.1128+7G>A rs200884259
NM_000238.3(KCNH2):c.1129-244G>A
NM_000238.3(KCNH2):c.1149C>T (p.Asp383=) rs201995634
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.1353G>A (p.Pro451=) rs763446458
NM_000238.3(KCNH2):c.1437C>T (p.Asn479=) rs188818227
NM_000238.3(KCNH2):c.1467C>T (p.Ile489=) rs740952
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.1581G>A (p.Ala527=) rs150275982
NM_000238.3(KCNH2):c.1598T>G (p.Val533Gly) rs202102276
NM_000238.3(KCNH2):c.1635C>T (p.Tyr545=) rs200692436
NM_000238.3(KCNH2):c.1683G>A (p.Ala561=) rs140366118
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=) rs41307295
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.2145+39G>C
NM_000238.3(KCNH2):c.2145+40G>A
NM_000238.3(KCNH2):c.2146-16C>T rs375568514
NM_000238.3(KCNH2):c.2190G>A (p.Leu730=) rs1401248493
NM_000238.3(KCNH2):c.2331C>T (p.Thr777=) rs41307292
NM_000238.3(KCNH2):c.2454G>A (p.Ser818=) rs72549418
NM_000238.3(KCNH2):c.2593-51C>T
NM_000238.3(KCNH2):c.2607G>A (p.Pro869=) rs199828796
NM_000238.3(KCNH2):c.2690A>C (p.Lys897Thr) rs1805123
NM_000238.3(KCNH2):c.2692+32C>G
NM_000238.3(KCNH2):c.2904G>A (p.Pro968=) rs75005975
NM_000238.3(KCNH2):c.2994C>T (p.Phe998=) rs368954514
NM_000238.3(KCNH2):c.300G>T (p.Arg100=) rs761176105
NM_000238.3(KCNH2):c.3063C>T (p.Ser1021=) rs199767579
NM_000238.3(KCNH2):c.308-271C>T
NM_000238.3(KCNH2):c.3111C>T (p.Asp1037=) rs200799870
NM_000238.3(KCNH2):c.3133C>T (p.Leu1045Phe) rs199473025
NM_000238.3(KCNH2):c.3140G>T (p.Arg1047Leu) rs36210421
NM_000238.3(KCNH2):c.3152+12C>A rs72549420
NM_000238.3(KCNH2):c.3153-15C>T rs41313755
NM_000238.3(KCNH2):c.3153-4C>T rs181119727
NM_000238.3(KCNH2):c.3216G>A (p.Thr1072=) rs200182770
NM_000238.3(KCNH2):c.3228C>T (p.Pro1076=) rs41312087
NM_000238.3(KCNH2):c.3331-13GT[2] rs41313749
NM_000238.3(KCNH2):c.3331-13del rs794728348
NM_000238.3(KCNH2):c.3331-14del rs794728347
NM_000238.3(KCNH2):c.3348G>A (p.Ala1116=) rs376180501
NM_000238.3(KCNH2):c.3366G>A (p.Pro1122=) rs371473271
NM_000238.3(KCNH2):c.342C>T (p.Pro114=) rs532959204
NM_000238.3(KCNH2):c.442C>T (p.Arg148Trp) rs139544114
NM_000238.3(KCNH2):c.472+78C>T
NM_000238.3(KCNH2):c.51C>G (p.Thr17=) rs144338227
NM_000238.3(KCNH2):c.542G>A (p.Arg181Gln) rs41308954
NM_000238.3(KCNH2):c.551_559GCGCGGGCG[1] (p.184_186GAG[1]) rs551056698
NM_000238.3(KCNH2):c.558C>T (p.Gly186=) rs139533994
NM_000238.3(KCNH2):c.568G>A (p.Ala190Thr) rs150817714
NM_000238.3(KCNH2):c.621C>T (p.Ser207=) rs41314417
NM_000238.3(KCNH2):c.76+161G>C
NM_000238.3(KCNH2):c.77-136dup
NM_000238.3(KCNH2):c.77-5C>G rs72549419
NM_000238.3(KCNH2):c.783G>A (p.Ser261=) rs769470521
NM_000238.3(KCNH2):c.817C>A (p.Arg273=) rs552583527
NM_000238.3(KCNH2):c.917-230A>G
NM_000238.3(KCNH2):c.982C>T (p.Arg328Cys) rs199473505
NM_172056.2(KCNH2):c.2414C>T (p.Ala805Val) rs201873431
NM_172056.2(KCNH2):c.2503del (p.Leu835fs) rs546898924
NM_172056.2(KCNH2):c.2553C>A (p.Ser851Arg) rs536958259
NM_172056.2(KCNH2):c.2576C>T (p.Thr859Met) rs41314366
NM_172056.2(KCNH2):c.2577G>A (p.Thr859=) rs373927190

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