ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.9854_9863del (p.Met3285fs)

dbSNP: rs398124105
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000582607 SCV000692216 pathogenic Duchenne muscular dystrophy 2015-09-14 no assertion criteria provided clinical testing
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000583821 SCV000692217 pathogenic Becker muscular dystrophy 2015-09-14 no assertion criteria provided clinical testing

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