List of variants reported as uncertain significance for Brugada syndrome by Agnes Ginges Centre for Molecular Cardiology, Centenary Institute

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000719.7(CACNA1C):c.4956+5G>C	rs758948589	0.00002
NM_000335.5(SCN5A):c.2441G>A (p.Arg814Gln)	rs199473584	0.00001
NM_000891.3(KCNJ2):c.83A>G (p.Asn28Ser)	rs2074384666
NM_001035.3(RYR2):c.4235A>G (p.Asp1412Gly)	rs1553515461
NM_001040151.2(SCN3B):c.118C>T (p.Pro40Ser)	rs762633602

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