ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.102C>A (p.Cys34Ter)

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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 RCV004549037 SCV005043343 likely pathogenic Familial multiple meningioma 2024-05-14 criteria provided, single submitter clinical testing

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