ClinVar Miner

Submissions for variant NC_000022.11:g.41150384_41156982delinsTG

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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 RCV000851524 SCV000994584 pathogenic Abnormal facial shape; Intellectual disability; Postaxial polydactyly 2019-05-02 criteria provided, single submitter clinical testing

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