ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.1212del (p.Phe404fs)

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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 RCV004577633 SCV005061586 pathogenic Retinoblastoma 2024-06-20 criteria provided, single submitter clinical testing

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