ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.6599_6601del (p.Phe2200del)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003474416 SCV004211880 uncertain significance Familial cancer of breast 2023-10-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011331 SCV004826960 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 2023-04-27 criteria provided, single submitter clinical testing

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