ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2134G>A (p.Gly712Arg)

dbSNP: rs1555491635
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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 RCV001218215 SCV001390087 likely benign Landau-Kleffner syndrome 2023-08-30 criteria provided, single submitter clinical testing

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