ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.1038C>T (p.Ala346=)

gnomAD frequency: 0.00049  dbSNP: 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
Labcorp Genetics (formerly Invitae), Labcorp RCV000891972 SCV001035825 benign D-2-hydroxyglutaric aciduria 2 2024-12-13 criteria provided, single submitter clinical testing

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