ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.3503G>A (p.Arg1168Gln) (rs886039281)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000254573 SCV000321062 uncertain significance Epilepsy, familial focal, with variable foci 1 2016-04-13 no assertion criteria provided literature only

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