ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.882C>T (p.Ala294=) (rs190078206)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000194175 SCV000247594 benign not specified 2017-09-25 criteria provided, single submitter clinical testing
Invitae RCV000891972 SCV001035825 benign D-2-hydroxyglutaric aciduria 2 2019-12-31 criteria provided, single submitter clinical testing

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