ClinVar Miner

Submissions for variant NM_014159.7(SETD2):c.4464T>G (p.Asn1488Lys)

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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 RCV003127364 SCV003803934 likely benign Autism spectrum disorder 2022-08-08 criteria provided, single submitter clinical testing

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