List of variants reported as likely benign for long QT syndrome by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.526C>T (p.Arg176Trp)	rs36210422	0.00061
NM_000218.3(KCNQ1):c.1179G>T (p.Lys393Asn)	rs12720457	0.00053

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