ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1081C>T (p.Leu361=)

dbSNP: rs267604690
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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 RCV003047659 SCV003338740 likely benign Landau-Kleffner syndrome 2022-04-17 criteria provided, single submitter clinical testing

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