ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5636G>A (p.Trp1879Ter)

dbSNP: rs1603631244
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990644 SCV001141661 pathogenic Duchenne muscular dystrophy 2019-05-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001263658 SCV001441750 likely pathogenic Becker muscular dystrophy; Duchenne muscular dystrophy 2019-10-24 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.