ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.67+82C>G (rs189026060)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000045025 SCV000073038 benign not provided 2019-03-06 criteria provided, single submitter clinical testing
Vantari Genetics RCV000210775 SCV000267013 uncertain significance Hereditary cancer-predisposing syndrome 2016-02-04 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113083 SCV000146098 uncertain significance Breast-ovarian cancer, familial 2 2010-12-17 no assertion criteria provided clinical testing

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