ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.72+1G>T

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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 RCV003127240 SCV003803772 likely pathogenic Autism spectrum disorder 2020-09-30 criteria provided, single submitter clinical testing

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