ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.2950C>T (p.Arg984Trp)

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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 RCV003127274 SCV003803814 likely benign Autism spectrum disorder 2022-07-05 criteria provided, single submitter clinical testing

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