ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.493T>C (p.Cys165Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, Hannover Medical School RCV004525812 SCV005038629 likely pathogenic Multiple endocrine neoplasia, type 1 2024-04-26 criteria provided, single submitter clinical testing

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