ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.4196_4197insAA (p.Tyr1399Ter)

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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 RCV004577411 SCV005061415 likely pathogenic Autosomal dominant non-syndromic intellectual disability 2024-06-17 criteria provided, single submitter clinical testing

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