ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3987C>T (p.Tyr1329=)

gnomAD frequency: 0.00009  dbSNP: rs560284703
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000941299 SCV001087182 likely benign not provided 2024-01-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000941299 SCV001247936 likely benign not provided 2019-07-01 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826989 SCV002088428 likely benign Usher syndrome type 1B 2020-02-27 no assertion criteria provided 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.