ClinVar Miner

List of variants in gene KCNH2 reported as likely benign for Long QT syndrome 2

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Total variants: 13
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HGVS dbSNP
NM_000238.4(KCNH2):c.*190C>T
NM_000238.4(KCNH2):c.422C>T (p.Pro141Leu) rs199472864
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.1332G>A (p.Glu444=) rs9770044
NM_172056.2(KCNH2):c.1558-5C>T rs114186001
NM_172056.2(KCNH2):c.1581G>A (p.Ala527=) rs150275982
NM_172056.2(KCNH2):c.524C>A (p.Ala175Asp) rs776541110
NM_172056.2(KCNH2):c.783G>A (p.Ser261=) rs769470521
NM_172057.2(KCNH2):c.*112C>T rs28763994
NM_172057.2(KCNH2):c.*15G>A rs41313746
NM_172057.2(KCNH2):c.2132+12C>A rs72549420
NM_172057.2(KCNH2):c.2208C>T (p.Pro736=) rs41312087

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