ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8378G>T (p.Gly2793Val) (rs80359083)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000569751 SCV000668734 uncertain significance Hereditary cancer-predisposing syndrome 2016-12-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
Counsyl RCV000031741 SCV000786215 uncertain significance Breast-ovarian cancer, familial 2 2018-03-23 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031741 SCV000054348 uncertain significance Breast-ovarian cancer, familial 2 2013-01-04 no assertion criteria provided clinical testing

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