ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8732C>T (p.Ala2911Val) (rs80359130)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000223485 SCV000275292 uncertain significance Hereditary cancer-predisposing syndrome 2015-04-23 criteria provided, single submitter clinical testing Insufficient or inconclusive evidence
Integrated Genetics/Laboratory Corporation of America RCV000588455 SCV000695172 uncertain significance not provided 2016-03-01 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000588455 SCV000889163 uncertain significance not provided 2018-05-11 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113990 SCV000147445 uncertain significance Breast-ovarian cancer, familial 2 2004-02-20 no assertion criteria provided clinical testing

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