ClinVar Miner

Submissions for variant NM_005592.4(MUSK):c.920+25del

dbSNP: rs147974075
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
PreventionGenetics, part of Exact Sciences RCV000249581 SCV000311145 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668514 SCV001888654 benign not provided 2018-06-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775748 SCV002014302 benign Fetal akinesia deformation sequence 1 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775749 SCV002014303 benign Congenital myasthenic syndrome 9 2021-09-05 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.