ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.316+1G>A (rs397507303)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000772114 SCV000905175 likely pathogenic Hereditary cancer-predisposing syndrome 2018-07-26 criteria provided, single submitter clinical testing
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge RCV000031403 SCV000326819 pathogenic Breast-ovarian cancer, familial 2 2015-10-02 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031403 SCV000054008 pathogenic Breast-ovarian cancer, familial 2 2009-01-22 no assertion criteria provided clinical testing

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