ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7772A>G (p.Asn2591Ser) (rs80359006)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Diagnosis of Cancer,West China Hospital, Sichuan University RCV000240696 SCV000265961 uncertain significance Neoplasm of the breast 2015-11-01 criteria provided, single submitter research
Institute for Biomarker Research,Medical Diagnostic Laboratories, L.L.C. RCV000677097 SCV000803158 uncertain significance Hereditary cancer-predisposing syndrome 2018-05-23 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113816 SCV000147179 uncertain significance Breast-ovarian cancer, familial 2 2003-12-23 no assertion criteria provided clinical testing

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