ClinVar Miner

Submissions for variant NM_000267.3:c.(?_-383)_(60+1_61-1)del

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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, University of Zurich RCV003107999 SCV002569060 pathogenic Neurofibromatosis, type 1 2022-05-25 criteria provided, single submitter clinical testing

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