ClinVar Miner

Submissions for variant NM_001385012.1(NBEA):c.5206dup (p.Ser1736fs)

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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 RCV003127402 SCV003803974 pathogenic Autism spectrum disorder 2022-05-10 criteria provided, single submitter clinical testing

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