ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3219del (p.Glu1073fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV003227556 SCV003924035 likely pathogenic Landau-Kleffner syndrome 2023-04-12 criteria provided, single submitter clinical testing

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