ClinVar Miner

Submissions for variant NM_030632.3(ASXL3):c.5221T>G (p.Ser1741Ala)

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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 RCV003127458 SCV003804042 likely benign Autism spectrum disorder 2021-03-26 criteria provided, single submitter clinical testing

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