List of variants in gene VCL reported as uncertain significance for Primary familial dilated 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.1555A>C (p.Ile519Leu)	rs141033098	0.00064
NM_014000.3(VCL):c.2827C>G (p.Pro943Ala)	rs71579375	0.00013
NM_014000.3(VCL):c.829C>A (p.Leu277Met)	rs71579353	0.00010
NM_014000.3(VCL):c.1621C>G (p.Leu541Val)	rs370229150	0.00008
NM_014000.3(VCL):c.163G>T (p.Val55Phe)	rs755441334	0.00001
NM_014000.3(VCL):c.2935A>G (p.Lys979Glu)	rs1591718331

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