ClinVar Miner

List of variants in gene KCNH2 studied for short QT syndrome

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Total variants: 5
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HGVS dbSNP
NM_000238.3(KCNH2):c.150G>T (p.Glu50Asp) rs199472841
NM_000238.3(KCNH2):c.1764C>A (p.Asn588Lys) rs104894021
NM_000238.3(KCNH2):c.1764C>G (p.Asn588Lys) rs104894021
NM_000238.3(KCNH2):c.1853C>T (p.Thr618Ile) rs199472947
NM_000238.3(KCNH2):c.3404G>A (p.Arg1135His) rs199473547

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