ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.4668C>A (p.Gly1556=) (rs762762532)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV000770471 SCV000901914 uncertain significance Cardiomyopathy 2016-04-28 criteria provided, single submitter clinical testing
Invitae RCV000865427 SCV001006388 likely benign Hypertrophic cardiomyopathy 2020-09-26 criteria provided, single submitter clinical testing
Color Health, Inc RCV000770471 SCV001347473 likely benign Cardiomyopathy 2018-12-31 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV001311856 SCV001502193 likely benign not provided 2020-11-01 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.