ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7805+23G>A (rs113653200)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409932 SCV000488808 likely benign Breast-ovarian cancer, familial 2 2016-06-20 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503496 SCV000592143 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing
Institute for Biomarker Research,Medical Diagnostic Laboratories, L.L.C. RCV000578018 SCV000679724 likely benign Hereditary cancer-predisposing syndrome 2017-07-12 criteria provided, single submitter clinical testing
Mendelics RCV000409932 SCV001139194 likely benign Breast-ovarian cancer, familial 2 2019-05-28 criteria provided, single submitter clinical testing

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