ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.5965C>G (p.Arg1989Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine RCV003647244 SCV004543826 likely pathogenic Intellectual disability, autosomal dominant 14 2023-07-05 criteria provided, single submitter clinical testing

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