ClinVar Miner

Submissions for variant NM_001079872.2(CUL4B):c.1444-1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV003484524 SCV004229080 likely pathogenic X-linked intellectual disability Cabezas type 2023-11-29 criteria provided, single submitter clinical testing

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