ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1122+15G>A

gnomAD frequency: 0.00003  dbSNP: rs770481323
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002108399 SCV002436387 likely benign Landau-Kleffner syndrome 2024-11-18 criteria provided, single submitter clinical testing

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