ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.8841G>A (p.Leu2947=)

gnomAD frequency: 0.00166  dbSNP: rs201809145
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
Eurofins Ntd Llc (ga) RCV000596759 SCV000706957 likely benign not specified 2017-03-30 criteria provided, single submitter clinical testing
GeneDx RCV000842023 SCV000984016 likely benign not provided 2021-09-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000842023 SCV001079096 benign not provided 2025-01-06 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.