List of variants reported as likely pathogenic for Brugada syndrome 3

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000719.7(CACNA1C):c.1832T>C (p.Met611Thr)
NM_000719.7(CACNA1C):c.3487G>A (p.Gly1163Ser)
NM_000719.7(CACNA1C):c.722T>C (p.Val241Ala)	rs2099444326
NM_000719.7(CACNA1C):c.794T>A (p.Met265Lys)
NM_001167623.2(CACNA1C):c.1216G>A (p.Gly406Arg)	rs786205745

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