ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1374G>A (p.Gly458=)

dbSNP: rs368221866
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192889 SCV000247521 uncertain significance not specified 2015-02-13 criteria provided, single submitter clinical testing
Invitae RCV002517078 SCV002963931 likely benign Landau-Kleffner syndrome 2023-11-24 criteria provided, single submitter clinical testing

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