ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.67+62T>G (rs11571574)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000503004 SCV000602748 benign not specified 2017-05-01 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113082 SCV000146097 uncertain significance Breast-ovarian cancer, familial 2 2010-12-17 no assertion criteria provided clinical testing
Color RCV000582922 SCV000688994 benign Hereditary cancer-predisposing syndrome 2015-03-11 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503004 SCV000591656 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing

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