ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.1265G>A (p.Arg422Gln) (rs886039277)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000711428 SCV000841793 uncertain significance not provided 2018-08-15 criteria provided, single submitter clinical testing
GeneReviews RCV000254583 SCV000321051 uncertain significance Epilepsy, familial focal, with variable foci 1 2016-04-13 no assertion criteria provided literature only

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