ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7617+4T>C (rs397507923)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000130854 SCV000185753 uncertain significance Hereditary cancer-predisposing syndrome 2018-02-07 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Color RCV000130854 SCV000906559 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-18 criteria provided, single submitter clinical testing
Invitae RCV000045262 SCV000073275 uncertain significance Hereditary breast and ovarian cancer syndrome 2017-08-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508569 SCV000600760 uncertain significance not specified 2017-02-06 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000083139 SCV000115213 uncertain significance Breast-ovarian cancer, familial 2 2013-07-01 no assertion criteria provided clinical testing

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