ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7561A>G (p.Ile2521Val) (rs80358983)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000219637 SCV000275145 uncertain significance Hereditary cancer-predisposing syndrome 2015-04-16 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113776 SCV000147123 uncertain significance Breast-ovarian cancer, familial 2 2004-02-20 no assertion criteria provided clinical testing

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