ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.4675+3A>T (rs80358082)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA1) RCV000112378 SCV000145146 pathogenic Breast-ovarian cancer, familial 1 2004-11-25 no assertion criteria provided clinical testing
Color RCV000772124 SCV000905200 likely pathogenic Hereditary cancer-predisposing syndrome 2018-07-29 criteria provided, single submitter clinical testing
Research Molecular Genetics Laboratory,Women's College Hospital, University of Toronto RCV000496914 SCV000587417 pathogenic Hereditary breast and ovarian cancer syndrome 2014-01-31 no assertion criteria provided research

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