ClinVar Miner

Submissions for variant NM_000827.4(GRIA1):c.1444G>T (p.Val482Phe)

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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 RCV003127235 SCV003803765 likely benign Autism spectrum disorder 2021-08-13 criteria provided, single submitter clinical testing

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