ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.9551dup (p.Asn3184fs)

dbSNP: rs863225017
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000201051 SCV000255760 pathogenic Duchenne muscular dystrophy 2015-01-16 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003488458 SCV004234441 pathogenic not provided 2023-04-14 criteria provided, single submitter clinical testing

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