ClinVar Miner

Submissions for variant NM_015015.3(KDM4B):c.2550+2T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV003447849 SCV004175741 likely pathogenic Intellectual developmental disorder, autosomal dominant 65 2023-12-12 criteria provided, single submitter clinical testing

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