ClinVar Miner

List of variants in gene KCNH2 reported as uncertain significance for Long QT syndrome 2

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Total variants: 18
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HGVS dbSNP
NM_000238.3(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_000238.3(KCNH2):c.1342G>T (p.Ala448Ser) rs767723985
NM_000238.3(KCNH2):c.1603G>A (p.Val535Met) rs375872367
NM_000238.3(KCNH2):c.1918T>C (p.Phe640Leu) rs199473529
NM_000238.3(KCNH2):c.2536C>G (p.Pro846Ala) rs199473006
NM_000238.3(KCNH2):c.2660G>A (p.Arg887His) rs199473432
NM_000238.3(KCNH2):c.2681G>A (p.Arg894His) rs199473668
NM_000238.3(KCNH2):c.2738C>T (p.Ala913Val) rs77331749
NM_000238.3(KCNH2):c.2893G>A (p.Gly965Arg) rs199473015
NM_000238.3(KCNH2):c.3140G>T (p.Arg1047Leu) rs36210421
NM_000238.3(KCNH2):c.343G>A (p.Val115Met) rs150988911
NM_000238.3(KCNH2):c.398T>C (p.Met133Thr) rs794728353
NM_000238.3(KCNH2):c.491G>A (p.Arg164His) rs199472866
NM_000238.3(KCNH2):c.566G>T (p.Gly189Val)
NM_000238.3(KCNH2):c.863T>C (p.Ile288Thr) rs1563169608
NM_000238.3(KCNH2):c.865G>A (p.Glu289Lys) rs199472880
NM_000238.3(KCNH2):c.872T>G (p.Met291Arg) rs199472881
NM_172057.2(KCNH2):c.78C>T (p.Ala26=) rs200324802

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