ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7488_7490GAA[1] (p.Lys2498del) (rs80359655)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000773270 SCV000906937 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-06 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113769 SCV000147106 uncertain significance Breast-ovarian cancer, familial 2 no assertion criteria provided clinical testing

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