ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.9117+9C>T (rs81002869)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA2) RCV000114052 SCV000147545 uncertain significance Breast-ovarian cancer, familial 2 2004-02-20 no assertion criteria provided clinical testing
Color RCV000773276 SCV000906959 likely benign Hereditary cancer-predisposing syndrome 2018-06-13 criteria provided, single submitter clinical testing
Counsyl RCV000114052 SCV000488217 likely benign Breast-ovarian cancer, familial 2 2016-01-27 criteria provided, single submitter clinical testing
Invitae RCV000045724 SCV000073737 likely benign Hereditary breast and ovarian cancer syndrome 2017-12-18 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507583 SCV000600844 likely benign not specified 2017-02-08 criteria provided, single submitter clinical testing

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