ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.1383C>T (p.Ala461=)

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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 RCV002761482 SCV003028986 likely benign Familial focal epilepsy with variable foci 2023-08-17 criteria provided, single submitter clinical testing

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