ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.2814C>G (p.Gly938=) rs2131956 0.73000
NM_014000.3(VCL):c.2388G>A (p.Pro796=) rs767809 0.42862
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.1407C>T (p.Ala469=) rs2229507 0.06287
NM_014000.3(VCL):c.1506G>A (p.Arg502=) rs2228373 0.06285
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180 0.02850
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179 0.00763
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.1671C>T (p.Asp557=) rs137877092 0.00228
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900 0.00051
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00034
NM_014000.3(VCL):c.1164C>T (p.Ile388=) rs370852950 0.00006
NM_014000.3(VCL):c.1575A>C (p.Glu525Asp) rs548487697
NM_014000.3(VCL):c.2560C>T (p.Leu854=) rs551463686

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.