ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.2919C>A (p.Pro973=)

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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 RCV005121488 SCV005746345 likely benign Familial focal epilepsy with variable foci 2024-03-05 criteria provided, single submitter clinical testing

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