ClinVar Miner

Submissions for variant NM_015267.4(CUX2):c.560del (p.Lys187fs)

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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, University of Goettingen RCV003224764 SCV003919744 likely pathogenic Developmental and epileptic encephalopathy, 67 2023-04-27 criteria provided, single submitter clinical testing

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