ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.626G>A (p.Arg209His) (rs118101777)

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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 RCV000193667 SCV000247599 likely benign not specified 2014-10-17 criteria provided, single submitter clinical testing
Invitae RCV000887014 SCV001030551 benign D-2-hydroxyglutaric aciduria 2 2019-12-31 criteria provided, single submitter clinical testing

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