ClinVar Miner

List of variants reported as likely pathogenic for Brugada syndrome by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.3908C>T (p.Thr1303Met)	rs199473603	0.00021
NM_000335.5(SCN5A):c.4219G>A (p.Gly1407Arg)	rs137854612

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