ClinVar Miner

Submissions for variant NM_001306215.2(ZNF827):c.590T>A (p.Leu197Ter)

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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 RCV003128022 SCV003804096 uncertain significance Autism spectrum disorder 2022-08-25 criteria provided, single submitter clinical testing

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