ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1965C>T (p.Val655=)

gnomAD frequency: 0.00001  dbSNP: rs1255068879
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001442859 SCV001645814 likely benign Duchenne muscular dystrophy 2024-02-09 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826262 SCV002092207 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2021-06-20 no assertion criteria provided clinical testing

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