ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.946+17G>A

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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 RCV002628084 SCV003509561 benign Familial focal epilepsy with variable foci 2025-01-13 criteria provided, single submitter clinical testing

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