List of variants in gene VCL reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.1907A>G (p.His636Arg)	rs71579374	0.00145
NM_014000.3(VCL):c.829C>A (p.Leu277Met)	rs71579353	0.00010
NM_014000.3(VCL):c.2046A>T (p.Leu682Phe)	rs565398652	0.00005
NM_014000.3(VCL):c.853C>T (p.Arg285Cys)	rs757517552	0.00002
NM_014000.3(VCL):c.1575A>C (p.Glu525Asp)	rs548487697

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