List of variants reported as uncertain significance for Brugada syndrome 1; Long QT syndrome 3 by Clinical Genomics Laboratory, Stanford Medicine

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.659C>T (p.Thr220Ile)	rs45620037	0.00064
NM_000335.5(SCN5A):c.53G>A (p.Arg18Gln)	rs41311087	0.00004
NM_000335.5(SCN5A):c.1939G>T (p.Ala647Ser)	rs753232371	0.00001
NM_000335.5(SCN5A):c.3301G>A (p.Ala1101Thr)	rs1481582794	0.00001

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