ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1786C>A (p.Pro596Thr)

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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 RCV003232045 SCV003930317 uncertain significance Familial cancer of breast 2023-06-09 criteria provided, single submitter clinical testing

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