ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.426-12G>A (rs81002880)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000230902 SCV000283232 likely benign not provided 2018-12-05 criteria provided, single submitter clinical testing
Color RCV000579640 SCV000683607 likely benign Hereditary cancer-predisposing syndrome 2016-02-10 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113565 SCV000146816 uncertain significance Breast-ovarian cancer, familial 2 2002-05-29 no assertion criteria provided clinical testing

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