ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2356+10C>T

gnomAD frequency: 0.00004  dbSNP: rs780647266
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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 RCV000872397 SCV001014199 likely benign Landau-Kleffner syndrome 2023-10-03 criteria provided, single submitter clinical testing

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