ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1032C>G (p.Tyr344Ter)

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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 RCV003986090 SCV004801952 pathogenic Nephroblastoma 2024-03-26 criteria provided, single submitter clinical testing

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