ClinVar Miner

Submissions for variant NM_002168.3(IDH2):c.673G>A (p.Asp225Asn) (rs142816010)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
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.
Genetic Services Laboratory, University of Chicago RCV000192325 SCV000247598 likely benign not specified 2015-03-06 criteria provided, single submitter clinical testing

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