List of variants reported as likely pathogenic for long QT syndrome by Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.1127G>A (p.Arg376His)	rs199473101	0.00003
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000218.3(KCNQ1):c.771_775dup (p.Arg259fs)	rs2133730742

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