ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1574C>G (p.Thr525Ser) (rs397507271)

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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 RCV000509790 SCV000607855 uncertain significance Hereditary cancer-predisposing syndrome 2016-01-20 criteria provided, single submitter clinical testing
Color RCV000509790 SCV000904082 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-26 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000239200 SCV000296539 uncertain significance Breast-ovarian cancer, familial 2 2016-04-08 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759576 SCV000888983 uncertain significance not provided 2018-05-03 criteria provided, single submitter clinical testing

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