ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1909+22del (rs276174816)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000043921 SCV000071934 benign Hereditary breast and ovarian cancer syndrome 2018-01-15 criteria provided, single submitter clinical testing
Counsyl RCV000119249 SCV000154100 benign Breast-ovarian cancer, familial 2 2014-04-10 criteria provided, single submitter literature only
Cancer Genetics and Genomics Laboratory,British Columbia Cancer Agency RCV000496608 SCV000586932 benign not specified 2017-04-18 criteria provided, single submitter clinical testing
Department of Pathology and Molecular Medicine,Queen's University RCV000496608 SCV000588081 uncertain significance not specified 2017-04-20 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000496608 SCV000602806 benign not specified 2016-11-12 criteria provided, single submitter clinical testing
Color RCV000580530 SCV000683457 likely benign Hereditary cancer-predisposing syndrome 2015-03-11 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000119249 SCV000743268 benign Breast-ovarian cancer, familial 2 2014-10-09 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000119249 SCV000145974 uncertain significance Breast-ovarian cancer, familial 2 1999-04-12 no assertion criteria provided clinical testing

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