ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.3330+5G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Génétique des Maladies du Développement, Hospices Civils de Lyon RCV001004711 SCV001164176 uncertain significance Epilepsy, familial focal, with variable foci 1 2017-12-29 criteria provided, single submitter clinical testing

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