ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2844del (p.Gln950fs)

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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, University of Leipzig Medical Center RCV003228787 SCV003925660 uncertain significance Landau-Kleffner syndrome 2023-04-18 criteria provided, single submitter clinical testing Criteria applied: PM2_SUP

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