ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3246C>G (p.Thr1082=)

dbSNP: rs143039009
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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 RCV000503330 SCV000595060 likely benign not specified 2016-02-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001470992 SCV001675093 likely benign Landau-Kleffner syndrome 2024-07-24 criteria provided, single submitter clinical testing

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