List of variants reported as benign for Primary dilated cardiomyopathy by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.1375G>A (p.Val459Ile)	rs73991549	0.00981
NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn)	rs121908338	0.00584
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg)	rs45550635	0.00271
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00269
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244

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.