ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.588C>T (p.Phe196=)

dbSNP: rs758536587
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002721280 SCV003006900 likely benign D-2-hydroxyglutaric aciduria 2 2022-07-05 criteria provided, single submitter clinical testing

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