List of variants in gene VCL reported as benign for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.768T>C (p.Asp256=)	rs56413529	0.06776
NM_014000.3(VCL):c.339G>A (p.Arg113=)	rs56314318	0.06767
NM_014000.3(VCL):c.945C>A (p.Gly315=)	rs61731180	0.02850
NM_014000.3(VCL):c.2801C>T (p.Ala934Val)	rs16931179	0.00658
NM_014000.3(VCL):c.1557C>A (p.Ile519=)	rs150120464	0.00466
NM_014000.3(VCL):c.1317T>C (p.Ser439=)	rs71579355	0.00442
NM_014000.3(VCL):c.1542C>T (p.Val514=)	rs7904077	0.00380
NM_014000.3(VCL):c.3258+10A>T	rs71579379	0.00267
NM_014000.3(VCL):c.2025G>A (p.Val675=)	rs140766884	0.00256
NM_014000.3(VCL):c.1671C>T (p.Asp557=)	rs137877092	0.00228
NM_014000.3(VCL):c.660C>T (p.Asn220=)	rs56264452	0.00091
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu)	rs141033098	0.00064
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.378C>T (p.Phe126=)	rs148966602	0.00012
NM_014000.3(VCL):c.1290C>T (p.Asp430=)	rs576271894	0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=)	rs147415627	0.00008
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg)	rs200342284
NM_014000.3(VCL):c.622+4C>T	rs201020802

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