List of variants reported as pathogenic for Atrial fibrillation, familial, 3; Long QT syndrome 1; Jervell and Lange-Nielsen syndrome 1; Short QT syndrome type 2

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1781G>A (p.Arg594Gln)	rs199472815	0.00001
NM_000218.3(KCNQ1):c.502G>A (p.Gly168Arg)	rs179489	0.00001
NM_000218.3(KCNQ1):c.568C>T (p.Arg190Trp)	rs199473662
NM_000218.3(KCNQ1):c.744G>A (p.Trp248Ter)

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