ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.3331-10del

gnomAD frequency: 0.00042  dbSNP: rs377356885
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001078651 SCV000286372 likely benign Familial focal epilepsy with variable foci 2025-01-06 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000711435 SCV000841800 benign not provided 2018-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000711435 SCV001867772 benign not provided 2019-03-29 criteria provided, single submitter clinical testing

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