ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.403del (p.Ala135fs)

dbSNP: rs2078781062
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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 Leipzig Medical Center RCV001253394 SCV001429076 likely pathogenic Familial cancer of breast 2018-07-09 criteria provided, single submitter clinical testing

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