ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.67+17T>C (rs767648965)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000195886 SCV000252611 benign Hereditary breast and ovarian cancer syndrome 2017-11-26 criteria provided, single submitter clinical testing
Counsyl RCV000411866 SCV000488200 uncertain significance Breast-ovarian cancer, familial 2 2016-01-24 criteria provided, single submitter clinical testing
Color RCV000580372 SCV000683800 likely benign Hereditary cancer-predisposing syndrome 2017-05-04 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679181 SCV000805750 likely benign not provided 2017-08-31 criteria provided, single submitter clinical testing

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