ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.68-7del (rs276174878)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000045052 SCV000073065 benign Hereditary breast and ovarian cancer syndrome 2017-12-26 criteria provided, single submitter clinical testing
Institute for Biomarker Research,Medical Diagnostic Laboratories, L.L.C. RCV000045052 SCV000267840 uncertain significance Hereditary breast and ovarian cancer syndrome 2016-04-25 criteria provided, single submitter clinical testing
Department of Pathology and Molecular Medicine,Queen's University RCV000496763 SCV000588066 uncertain significance not specified 2017-04-20 criteria provided, single submitter clinical testing
Color RCV000580115 SCV000683811 benign Hereditary cancer-predisposing syndrome 2016-09-16 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113085 SCV000146101 uncertain significance Breast-ovarian cancer, familial 2 no assertion criteria provided clinical testing

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