ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5749C>A (p.Arg1917=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003512832 SCV004364878 likely benign Duchenne muscular dystrophy 2023-12-10 criteria provided, single submitter clinical testing

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