ClinVar Miner

Submissions for variant NM_152641.4(ARID2):c.4693G>A (p.Val1565Ile)

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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 RCV003127267 SCV003803805 likely benign Autism spectrum disorder 2022-07-28 criteria provided, single submitter clinical testing

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