ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=)

gnomAD frequency: 0.00001  dbSNP: rs587780352
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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 RCV000117177 SCV000151341 likely benign not specified 2014-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001506548 SCV001711471 likely benign Landau-Kleffner syndrome 2024-11-18 criteria provided, single submitter clinical testing

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