ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.1078+19dup

dbSNP: rs144408691
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246807 SCV000310764 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000293454 SCV000465376 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV004577737 SCV000465377 likely benign Hearing loss, autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001610655 SCV001832997 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001610655 SCV002453358 benign not provided 2025-02-02 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.