ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.4437-15C>G

dbSNP: rs755374231
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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 RCV002118015 SCV002406823 benign Familial focal epilepsy with variable foci 2024-05-15 criteria provided, single submitter clinical testing

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