List of variants reported as likely pathogenic for Long QT syndrome 2 by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.1052C>T (p.Ser351Leu)	rs759134380	0.00001
NM_000238.4(KCNH2):c.2053C>T (p.Arg685Cys)	rs778135438	0.00001
NM_000238.4(KCNH2):c.1238T>G (p.Leu413Arg)	rs199472893
NM_000238.4(KCNH2):c.139G>T (p.Gly47Cys)	rs794728409
NM_000238.4(KCNH2):c.1469C>T (p.Ala490Val)	rs1801214475
NM_000238.4(KCNH2):c.146G>T (p.Cys49Phe)	rs199472840
NM_000238.4(KCNH2):c.1525G>A (p.Asp509Asn)	rs370637245
NM_000238.4(KCNH2):c.1838C>T (p.Thr613Met)	rs199473524
NM_000238.4(KCNH2):c.1910AGA[1] (p.Lys638del)	rs794728442
NM_000238.4(KCNH2):c.92T>A (p.Ile31Asn)	rs199472833

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