ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8958A>G (p.Ile2986Met) (rs398122719)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218696 SCV000274610 uncertain significance Hereditary cancer-predisposing syndrome 2015-03-23 criteria provided, single submitter clinical testing
Color RCV000218696 SCV000689163 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-30 criteria provided, single submitter clinical testing
Counsyl RCV000077649 SCV000785844 uncertain significance Breast-ovarian cancer, familial 2 2017-12-27 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077649 SCV000109452 uncertain significance Breast-ovarian cancer, familial 2 2009-11-19 no assertion criteria provided clinical testing

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