ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.76G>T (p.Ala26Ser)

gnomAD frequency: 0.00004  dbSNP: rs751198815
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000187633 SCV000241230 likely benign not provided 2021-01-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000545221 SCV000638254 likely benign Landau-Kleffner syndrome 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000187633 SCV005217452 likely benign not provided criteria provided, single submitter not provided

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