ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.135-8dup

dbSNP: rs397507186
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001176119 SCV001339967 likely benign Hereditary cancer-predisposing syndrome 2023-09-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001437751 SCV001640615 likely benign Hereditary breast ovarian cancer syndrome 2021-10-27 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001176119 SCV002538016 uncertain significance Hereditary cancer-predisposing syndrome 2021-05-19 criteria provided, single submitter curation
All of Us Research Program, National Institutes of Health RCV000030986 SCV004828697 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2023-09-17 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000030986 SCV000053578 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2011-06-01 no assertion criteria provided clinical testing
BRCAlab, Lund University RCV000030986 SCV004244191 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2020-03-02 no assertion criteria provided clinical testing

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