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

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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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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