ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.670+8C>T (rs80358050)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA1) RCV000031273 SCV000145653 uncertain significance Breast-ovarian cancer, familial 1 2004-02-20 no assertion criteria provided clinical testing
Color RCV000581155 SCV000688655 likely benign Hereditary cancer-predisposing syndrome 2016-08-05 criteria provided, single submitter clinical testing
Department of Pathology and Molecular Medicine,Queen's University RCV000496492 SCV000588031 likely benign not specified 2017-04-20 criteria provided, single submitter clinical testing
Invitae RCV000049088 SCV000077101 uncertain significance Hereditary breast and ovarian cancer syndrome 2015-09-30 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031273 SCV000053878 likely benign Breast-ovarian cancer, familial 1 2009-06-24 no assertion criteria provided clinical testing

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