ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.4738dup (p.Cys1580fs)

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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 Human Genetics, University of Goettingen RCV003128311 SCV003804454 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 2 2023-02-24 criteria provided, single submitter clinical testing

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