ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.3396+10C>A (rs755463750)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001088822 SCV000642192 likely benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000545790 SCV000743136 likely benign Epilepsy, familial focal, with variable foci 1 2015-09-24 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000545790 SCV000744146 likely benign Epilepsy, familial focal, with variable foci 1 2016-01-18 criteria provided, single submitter clinical testing

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