ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3978C>G (p.Gly1326=)

dbSNP: rs368066766
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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 RCV001415883 SCV001618052 likely benign Landau-Kleffner syndrome 2019-05-18 criteria provided, single submitter clinical testing

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