ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.894C>T (p.Thr298=) (rs11540478)

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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 RCV000146092 SCV000193309 likely benign not specified 2013-10-31 criteria provided, single submitter clinical testing
Invitae RCV000534348 SCV000650097 benign D-2-hydroxyglutaric aciduria 2 2019-12-31 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000676984 SCV000802811 benign not provided 2016-03-16 no assertion criteria provided clinical testing

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