ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10683G>A (p.Glu3561=)

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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 RCV002649282 SCV002960311 likely benign Duchenne muscular dystrophy 2022-08-22 criteria provided, single submitter clinical testing

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