ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1585del (p.Val529fs)

dbSNP: rs2141342590
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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 RCV001785253 SCV002026180 likely pathogenic Landau-Kleffner syndrome 2019-01-01 criteria provided, single submitter research

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