List of variants reported as likely pathogenic for Brugada syndrome by Center for Medical Genetics Ghent, University of Ghent

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.4531C>T (p.Arg1511Trp)	rs137854602	0.00001
NM_000335.5(SCN5A):c.5353_5354del (p.Leu1785fs)	rs886037903
NM_000335.5(SCN5A):c.844C>T (p.Arg282Cys)	rs199473082
NM_198056.2(SCN5A):c.4813+3_4813+6dup

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