ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.81-14C>G

dbSNP: rs80358006
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C. RCV000210969 SCV000267858 likely benign Hereditary breast ovarian cancer syndrome 2016-04-25 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000584417 SCV000688669 likely benign Hereditary cancer-predisposing syndrome 2016-12-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000210969 SCV001012075 likely benign Hereditary breast ovarian cancer syndrome 2023-12-17 criteria provided, single submitter clinical testing
Mendelics RCV000989917 SCV001140651 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2019-05-28 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000989917 SCV004016789 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2023-07-07 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000989917 SCV004827896 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2023-11-28 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV000989917 SCV001237808 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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