ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3909C>T (p.Asp1303=)

gnomAD frequency: 0.00004  dbSNP: rs765744766
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698257 SCV000532323 likely benign not provided 2019-09-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001396131 SCV001597854 likely benign Landau-Kleffner syndrome 2024-11-21 criteria provided, single submitter clinical testing

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