ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=)

gnomAD frequency: 0.00003  dbSNP: rs587780350
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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 RCV000117174 SCV000151338 likely benign not specified 2016-02-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001459471 SCV001663310 likely benign Landau-Kleffner syndrome 2024-10-30 criteria provided, single submitter clinical testing

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