ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5153-2A>C

dbSNP: rs786202545
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Program, Instituto Nacional de Cancer RCV002307682 SCV002515227 pathogenic Hereditary breast ovarian cancer syndrome 2021-11-01 criteria provided, single submitter research
Mendelics RCV002249674 SCV002518586 pathogenic Familial cancer of breast 2022-05-04 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077719 SCV001243688 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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