ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3567G>A (p.Lys1189=)

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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 RCV003089269 SCV003466232 likely benign Landau-Kleffner syndrome 2023-01-14 criteria provided, single submitter clinical testing

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