ClinVar Miner

Submissions for variant NM_000834.5(GRIN2B):c.3391del (p.Asp1131fs)

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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 Goettingen RCV004586469 SCV005073968 likely pathogenic Intellectual disability, autosomal dominant 6 2024-07-09 criteria provided, single submitter clinical testing

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