ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7805+8A>G (rs81002847)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA2) RCV000077413 SCV000147188 uncertain significance Breast-ovarian cancer, familial 2 no assertion criteria provided clinical testing
Color RCV000581094 SCV000683910 likely benign Hereditary cancer-predisposing syndrome 2015-09-03 criteria provided, single submitter clinical testing
Invitae RCV000045317 SCV000073330 likely benign Hereditary breast and ovarian cancer syndrome 2017-11-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507747 SCV000600768 likely benign not specified 2017-01-26 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758952 SCV000887925 likely benign not provided 2018-02-09 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077413 SCV000109211 likely benign Breast-ovarian cancer, familial 2 2010-07-22 no assertion criteria provided clinical testing

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