List of variants reported as likely benign for Brugada syndrome by Mendelics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val)	rs142653846	0.00318
NM_000335.5(SCN5A):c.3919C>T (p.Leu1307Phe)	rs41313031	0.00144
NM_006514.4(SCN10A):c.4984G>A (p.Gly1662Ser)	rs151090729	0.00047
NM_000335.5(SCN5A):c.4591G>A (p.Val1531Ile)	rs199473618	0.00021
NM_000335.5(SCN5A):c.80G>A (p.Arg27His)	rs199473045	0.00017
NM_000335.5(SCN5A):c.436G>A (p.Val146Met)	rs199473061	0.00002
NM_000335.5(SCN5A):c.5960T>G (p.Leu1987Arg)	rs145009013	0.00002
NM_000335.5(SCN5A):c.1372C>T (p.Arg458Cys)	rs752130196
NM_006514.4(SCN10A):c.1246AAG[1] (p.Lys417del)	rs758898721
NM_006514.4(SCN10A):c.41G>T (p.Arg14Leu)	rs141207048

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