ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.364-10C>T (rs116263417)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244822 SCV000307094 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000475913 SCV000558182 benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing

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