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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 222887	NM_014000.3(VCL):c.565G>A (p.Val189Met)	VCL (V189M)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +2 more	GUncertain significance
Select item 178980	NM_014000.3(VCL):c.610G>C (p.Val204Leu)	VCL (V204L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 45582	NM_014000.3(VCL):c.1555A>C (p.Ile519Leu)	VCL (I519L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +6 more	GConflicting classifications of pathogenicity
Select item 222888	NM_014000.3(VCL):c.1559G>A (p.Arg520Gln)	VCL (R520Q)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +3 more	GUncertain significance
Select item 45594	NM_014000.3(VCL):c.1907A>G (p.His636Arg)	VCL (H636R)	Single nucleotide variant (missense variant)	Primary familial hypertrophic cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 180585	NM_014000.3(VCL):c.2050A>G (p.Arg684Gly)	VCL (R684G)	Single nucleotide variant (missense variant)	Ventricular fibrillation, paroxysmal familial, type 1	GUncertain significance
Select item 222889	NM_014000.3(VCL):c.2468G>A (p.Arg823Gln)	VCL (R823Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity

ClinVar