ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3787G>A (p.Gly1263Arg)

gnomAD frequency: 0.00004  dbSNP: rs142113044
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001917260 SCV002154976 likely benign Landau-Kleffner syndrome 2024-10-24 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001917260 SCV003817446 uncertain significance Landau-Kleffner syndrome 2022-05-02 criteria provided, single submitter clinical testing

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