ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1845C>A (p.Asn615Lys)

dbSNP: rs397518447
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Total submissions: 3
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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 RCV000022585 SCV002026445 likely pathogenic Landau-Kleffner syndrome 2019-01-01 criteria provided, single submitter research
OMIM RCV000022585 SCV000043874 pathogenic Landau-Kleffner syndrome 2010-11-01 no assertion criteria provided literature only
GeneReviews RCV000022585 SCV000320742 not provided Landau-Kleffner syndrome no assertion provided literature only

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