ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2336T>G (p.Leu779Trp)

dbSNP: rs1555488084
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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 RCV001262726 SCV001440700 uncertain significance Landau-Kleffner syndrome 2019-01-01 criteria provided, single submitter clinical testing

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