List of variants reported as likely pathogenic for Brugada syndrome by Institute of Human Genetics, Heidelberg University

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.4856C>T (p.Thr1619Met)	rs199473282	0.00001
NM_201596.3(CACNB2):c.1604C>T (p.Ser535Leu)	rs121917812

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