ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.2567+8A>G (rs370009456)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001083976 SCV000642181 benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000711433 SCV000841798 benign not provided 2017-12-08 criteria provided, single submitter clinical testing

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