ClinVar Miner

List of variants reported as likely pathogenic for Brugada syndrome 5

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.448+88G>A	rs267607028	0.00001
NM_001037.5(SCN1B):c.40+1_40+50del	rs2064208734
NM_001037.5(SCN1B):c.449-1G>T
NM_001037.5(SCN1B):c.449-2A>G	rs1600370558

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