ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.426-37T>A (rs81002859)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000044382 SCV000072395 likely benign Hereditary breast and ovarian cancer syndrome 2016-03-14 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000501629 SCV000591681 likely benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000501629 SCV000602809 benign not specified 2016-10-13 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113568 SCV000146819 uncertain significance Breast-ovarian cancer, familial 2 1997-11-13 no assertion criteria provided clinical testing

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