List of variants reported as likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000218.3(KCNQ1):c.776G>A (p.Arg259His)	rs199472720	0.00001
NM_000218.3(KCNQ1):c.1257_1260del (p.Lys421fs)
NM_000218.3(KCNQ1):c.1685+2T>G	rs1590081467
NM_000218.3(KCNQ1):c.605-1G>C	rs1564820372
NM_000218.3(KCNQ1):c.771_775dup (p.Arg259fs)	rs2133730742

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