ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.517G>A (p.Asp173Asn) (rs142816010)

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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 RCV000192325 SCV000247598 likely benign not specified 2015-03-06 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000439729 SCV000510743 uncertain significance not provided 2016-11-22 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.
Invitae RCV001084682 SCV001131907 likely benign D-2-hydroxyglutaric aciduria 2 2019-12-31 criteria provided, single submitter clinical testing

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