List of variants in gene VCL reported as uncertain significance for Primary 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: 10

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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.1973T>C (p.Val658Ala)	rs372691803	0.00010
NM_014000.3(VCL):c.2531C>T (p.Pro844Leu)	rs145393322	0.00007
NM_014000.3(VCL):c.1961A>C (p.Asn654Thr)	rs1591709946	0.00001
NM_003373.4(VCL):c.670dup (p.Glu224fs)	rs876657674
NM_014000.3(VCL):c.1343T>C (p.Leu448Pro)	rs2549223382
NM_014000.3(VCL):c.1382C>A (p.Ala461Asp)	rs886038800
NM_014000.3(VCL):c.1639C>T (p.Arg547Ter)	rs397517234
NM_014000.3(VCL):c.2035G>T (p.Ala679Ser)	rs375392559
NM_014000.3(VCL):c.2882C>A (p.Pro961Gln)	rs754591130

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