List of variants reported as likely benign for Dilated cardiomyopathy 1W by Illumina Laboratory Services, Illumina

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.*1854A>C	rs3829204	0.11620
NM_014000.3(VCL):c.945C>A (p.Gly315=)	rs61731180	0.02850
NM_014000.3(VCL):c.*292G>C	rs77295081	0.01549
NM_014000.3(VCL):c.2801C>T (p.Ala934Val)	rs16931179	0.00763
NM_014000.3(VCL):c.*1203A>C	rs149551128	0.00511
NM_014000.3(VCL):c.*1636C>T	rs144240368	0.00453
NM_014000.3(VCL):c.1542C>T (p.Val514=)	rs7904077	0.00355
NM_014000.3(VCL):c.1671C>T (p.Asp557=)	rs137877092	0.00228
NM_014000.3(VCL):c.660C>T (p.Asn220=)	rs56264452	0.00094
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.*107T>A	rs76086805	0.00035

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.