ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8954-5_8954-2delAACA (rs587782878)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000132512 SCV000187608 benign Hereditary cancer-predisposing syndrome 2014-11-19 criteria provided, single submitter clinical testing
Color RCV000132512 SCV000684011 benign Hereditary cancer-predisposing syndrome 2016-06-21 criteria provided, single submitter clinical testing
Counsyl RCV000031782 SCV000487807 uncertain significance Breast-ovarian cancer, familial 2 2015-11-17 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503174 SCV000592243 uncertain significance not specified 2017-02-23 criteria provided, single submitter clinical testing
Invitae RCV000204559 SCV000261842 benign Hereditary breast and ovarian cancer syndrome 2018-01-05 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031782 SCV000054390 likely benign Breast-ovarian cancer, familial 2 2011-03-04 no assertion criteria provided clinical testing

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