ClinVar Miner

List of variants reported as uncertain significance for Dilated cardiomyopathy 1W by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.2969C>T (p.Ala990Val) rs150595117 0.00019
NM_014000.3(VCL):c.437C>T (p.Thr146Ile) rs1421034616 0.00001
NM_014000.3(VCL):c.2119G>A (p.Glu707Lys) rs2549231580
NM_014000.3(VCL):c.2569G>A (p.Glu857Lys) rs2549234256
NM_014000.3(VCL):c.323_327delinsAAGCAG (p.Leu108fs) rs2549212029
NM_014000.3(VCL):c.3250T>C (p.Ser1084Pro) rs1197638416

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.