List of variants in gene SCN1B reported as likely pathogenic for Brugada syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.373C>T (p.Arg125Cys)	rs1135401736	0.00001
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.448+201C>T	rs2151746638
NM_001037.5(SCN1B):c.449-1G>T
NM_001037.5(SCN1B):c.449-2A>G	rs1600370558

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