ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.360G>A (p.Glu120=)

gnomAD frequency: 0.00011  dbSNP: rs536071174
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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 RCV000501042 SCV000595216 likely benign not specified 2018-02-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000967630 SCV001115022 likely benign D-2-hydroxyglutaric aciduria 2 2024-04-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705628 SCV005213996 likely benign not provided criteria provided, single submitter not provided

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