ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.414+7C>T

gnomAD frequency: 0.00002  dbSNP: rs748888605
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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 RCV000687846 SCV000815435 likely benign Landau-Kleffner syndrome 2023-07-14 criteria provided, single submitter clinical testing

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