ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8954-16_8954-8del

dbSNP: rs398122718
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001447781 SCV001650854 likely benign Hereditary breast ovarian cancer syndrome 2024-04-11 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV002477221 SCV002774513 uncertain significance not provided 2021-09-02 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077648 SCV000109451 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 2010-11-03 no assertion criteria provided clinical testing

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