ClinVar Miner

List of variants in gene KCNH2 reported as benign for not specified

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Total variants: 36
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HGVS dbSNP
NM_172056.2(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_172056.2(KCNH2):c.1128+1784C>T rs371509270
NM_172056.2(KCNH2):c.1149C>T (p.Asp383=) rs201995634
NM_172056.2(KCNH2):c.1353G>A (p.Pro451=) rs763446458
NM_172056.2(KCNH2):c.1437C>T (p.Asn479=) rs188818227
NM_172056.2(KCNH2):c.1467C>T (p.Ile489=) rs740952
NM_172056.2(KCNH2):c.1528C>T (p.Leu510=) rs75648145
NM_172056.2(KCNH2):c.1539C>T (p.Phe513=) rs1805120
NM_172056.2(KCNH2):c.1581G>A (p.Ala527=) rs150275982
NM_172056.2(KCNH2):c.1598T>G (p.Val533Gly) rs202102276
NM_172056.2(KCNH2):c.1683G>A (p.Ala561=) rs140366118
NM_172056.2(KCNH2):c.1692A>G (p.Leu564=) rs1805121
NM_172056.2(KCNH2):c.1800C>T (p.Ser600=) rs143518632
NM_172056.2(KCNH2):c.1956T>C (p.Tyr652=) rs1137617
NM_172056.2(KCNH2):c.2146-16C>T rs375568514
NM_172056.2(KCNH2):c.2190G>A (p.Leu730=) rs1401248493
NM_172056.2(KCNH2):c.2414C>T (p.Ala805Val) rs201873431
NM_172056.2(KCNH2):c.2577G>A (p.Thr859=) rs373927190
NM_172056.2(KCNH2):c.342C>T (p.Pro114=) rs532959204
NM_172056.2(KCNH2):c.51C>G (p.Thr17=) rs144338227
NM_172056.2(KCNH2):c.558C>T (p.Gly186=) rs139533994
NM_172056.2(KCNH2):c.568G>A (p.Ala190Thr) rs150817714
NM_172056.2(KCNH2):c.783G>A (p.Ser261=) rs769470521
NM_172056.2(KCNH2):c.817C>A (p.Arg273=) rs552583527
NM_172057.2(KCNH2):c.1434G>A (p.Ser478=) rs72549418
NM_172057.2(KCNH2):c.1587G>A (p.Pro529=) rs199828796
NM_172057.2(KCNH2):c.1670A>C (p.Lys557Thr) rs1805123
NM_172057.2(KCNH2):c.1884G>A (p.Pro628=) rs75005975
NM_172057.2(KCNH2):c.1974C>T (p.Phe658=) rs368954514
NM_172057.2(KCNH2):c.2091C>T (p.Asp697=) rs200799870
NM_172057.2(KCNH2):c.2120G>T (p.Arg707Leu) rs36210421
NM_172057.2(KCNH2):c.2132+12C>A rs72549420
NM_172057.2(KCNH2):c.2133-15C>T rs41313755
NM_172057.2(KCNH2):c.2311-13GT[2] rs41313749
NM_172057.2(KCNH2):c.2328G>A (p.Ala776=) rs376180501
NM_172057.2(KCNH2):c.2346G>A (p.Pro782=) rs371473271

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