ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.1148C>T (p.Thr383Met) (rs118053940)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000146093 SCV000193310 likely benign not specified 2014-04-18 criteria provided, single submitter clinical testing
Invitae RCV001081553 SCV001107621 benign D-2-hydroxyglutaric aciduria 2 2019-12-31 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000676983 SCV000802810 likely benign not provided 2016-02-26 no assertion criteria provided clinical testing

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