ClinVar Miner

Submissions for variant NM_144573.3(NEXN):c.1422G>A (p.Arg474=) (rs775204901)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000546686 SCV000648476 likely benign not provided 2018-08-29 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV001170731 SCV001333334 benign Cardiomyopathy 2018-03-27 criteria provided, single submitter clinical testing
Invitae RCV001506161 SCV001711076 likely benign Dilated cardiomyopathy 1CC; Familial hypertrophic cardiomyopathy 20 2018-10-25 criteria provided, single submitter clinical testing

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.