ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7976+45G>C (rs11571718)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000501599 SCV000592162 likely benign not specified criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000211006 SCV000743338 likely benign Breast-ovarian cancer, familial 2 2014-10-09 criteria provided, single submitter clinical testing
Michigan Medical Genetics Laboratories,University of Michigan RCV000211006 SCV000267815 benign Breast-ovarian cancer, familial 2 2016-04-21 criteria provided, single submitter clinical testing
University of Washington Department of Laboratory Medicine,University of Washington RCV000209252 SCV000265012 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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