ClinVar Miner

List of variants in gene KCNH2 reported as benign for Long QT syndrome

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Total variants: 32
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HGVS dbSNP
NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_000238.4(KCNH2):c.1467C>T (p.Ile489=) rs740952
NM_000238.4(KCNH2):c.1539C>T (p.Phe513=) rs1805120
NM_000238.4(KCNH2):c.1563C>T (p.Ile521=) rs143011005
NM_000238.4(KCNH2):c.1692A>G (p.Leu564=) rs1805121
NM_000238.4(KCNH2):c.1956T>C (p.Tyr652=) rs1137617
NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr) rs1805123
NM_000238.4(KCNH2):c.3331-13GT[2] rs41313749
NM_000238.4(KCNH2):c.442C>T (p.Arg148Trp) rs139544114
NM_000238.4(KCNH2):c.551_559GCGCGGGCG[1] (p.184_186GAG[1]) rs551056698
NM_172056.2(KCNH2):c.1320G>T (p.Pro440=) rs144926928
NM_172056.2(KCNH2):c.1332G>A (p.Glu444=) rs9770044
NM_172056.2(KCNH2):c.1500C>A (p.Ile500=) rs147126965
NM_172056.2(KCNH2):c.1528C>T (p.Leu510=) rs75648145
NM_172056.2(KCNH2):c.1558-5C>T rs114186001
NM_172056.2(KCNH2):c.1581G>A (p.Ala527=) rs150275982
NM_172056.2(KCNH2):c.1635C>T (p.Tyr545=) rs200692436
NM_172056.2(KCNH2):c.1800C>T (p.Ser600=) rs143518632
NM_172056.2(KCNH2):c.1809C>T (p.Gly603=) rs41314375
NM_172056.2(KCNH2):c.2127C>T (p.Asn709=) rs768572372
NM_172056.2(KCNH2):c.2331C>T (p.Thr777=) rs41307292
NM_172056.2(KCNH2):c.300G>T (p.Arg100=) rs761176105
NM_172056.2(KCNH2):c.51C>G (p.Thr17=) rs144338227
NM_172056.2(KCNH2):c.542G>A (p.Arg181Gln) rs41308954
NM_172056.2(KCNH2):c.621C>T (p.Ser207=) rs41314417
NM_172056.2(KCNH2):c.982C>T (p.Arg328Cys) rs199473505
NM_172057.2(KCNH2):c.2043C>T (p.Ser681=) rs199767579
NM_172057.2(KCNH2):c.2113C>T (p.Leu705Phe) rs199473025
NM_172057.2(KCNH2):c.2120G>T (p.Arg707Leu) rs36210421
NM_172057.2(KCNH2):c.2133-4C>T rs181119727
NM_172057.2(KCNH2):c.2196G>A (p.Thr732=) rs200182770
NM_172057.2(KCNH2):c.2208C>T (p.Pro736=) rs41312087

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