"Blueprint Genetics"[submitter] AND "CACNB2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 222521	NM_201596.3(CACNB2):c.334-8C>T	CACNB2	Single nucleotide variant (intron variant)	Ventricular fibrillation +1 more	GConflicting classifications of pathogenicity
Select item 180289	NM_201596.3(CACNB2):c.1056G>A (p.Ala352=)	CACNB2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 191435	NM_201596.3(CACNB2):c.1206+4_1206+7dup	CACNB2	Duplication (splice donor variant)	Brugada syndrome 4 +4 more	GConflicting classifications of pathogenicity
Select item 180291	NM_201596.3(CACNB2):c.1206+3A>T	CACNB2	Single nucleotide variant (intron variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 222519	NM_201596.3(CACNB2):c.1399C>T (p.Pro467Ser)	CACNB2 (P413S +9 more)	Single nucleotide variant (missense variant)	Conduction system disorder	GUncertain significance
Select item 222520	NM_201596.3(CACNB2):c.1594T>G (p.Ser532Ala)	CACNB2 (S477A +9 more)	Single nucleotide variant (missense variant)	Cardiac arrest	GUncertain significance
Select item 180290	NM_201596.3(CACNB2):c.1642G>A (p.Gly548Ser)	CACNB2 (G494S +9 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

ClinVar