ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.2875C>T (p.Gln959Ter)

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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 Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn RCV004776539 SCV005387907 pathogenic Mowat-Wilson syndrome 2024-04-24 criteria provided, single submitter clinical testing

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