List of variants in gene CACNB2 reported as likely benign for Brugada syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_201596.3(CACNB2):c.214-61250G>A	rs10828545	0.40469
NM_201596.3(CACNB2):c.214-61251C>A	rs117558767	0.00589
NM_201596.3(CACNB2):c.641G>C (p.Ser214Thr)	rs149253719	0.00078

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