ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.681+56C>G

dbSNP: rs2126042
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Molecular Medicine, Queen's University RCV000496557 SCV000588068 benign not specified 2017-04-20 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000114010 SCV000147475 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 1999-06-22 no assertion criteria provided clinical testing

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