ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.968-10T>C

dbSNP: rs2505785937
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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 RCV003516146 SCV004344266 likely benign D-2-hydroxyglutaric aciduria 2 2023-06-27 criteria provided, single submitter clinical testing

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