ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.2193T>G (p.Leu731=)

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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 RCV002858547 SCV003234222 likely benign Duchenne muscular dystrophy 2022-09-15 criteria provided, single submitter clinical testing

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