ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.5993A>G (p.Gln1998Arg) (rs80358835)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503659 SCV000592020 uncertain significance not specified 2015-03-13 criteria provided, single submitter clinical testing
Color RCV000580157 SCV000683748 uncertain significance Hereditary cancer-predisposing syndrome 2018-09-29 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113517 SCV000146748 uncertain significance Breast-ovarian cancer, familial 2 2003-01-24 no assertion criteria provided clinical testing

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