List of variants in gene VCL reported as benign for hypertrophic cardiomyopathy

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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_014000.3(VCL):c.2814C>G (p.Gly938=)	rs2131956	0.74148
NM_014000.3(VCL):c.875-24T>A	rs1908339	0.65590
NM_014000.3(VCL):c.2388G>A (p.Pro796=)	rs767809	0.42862
NM_014000.3(VCL):c.3153+47T>C	rs2270550	0.42070
NM_014000.3(VCL):c.*1854A>C	rs3829204	0.11656
NM_014000.3(VCL):c.1557C>A (p.Ile519=)	rs150120464	0.00466

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