ClinVar Miner

List of variants in gene VCL reported as benign for Cardiovascular phenotype

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Total variants: 13
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HGVS dbSNP
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1407C>T (p.Ala469=) rs2229507
NM_014000.2(VCL):c.1506G>A (p.Arg502=) rs2228373
NM_014000.2(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.2388G>A (p.Pro796=) rs767809
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.2(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.2(VCL):c.2814C>G (p.Gly938=) rs2131956
NM_014000.2(VCL):c.339G>A (p.Arg113=) rs56314318
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.2(VCL):c.768T>C (p.Asp256=) rs56413529
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180

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