ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5333-36_5333-22del

dbSNP: rs1555575231
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005398716 SCV006058353 likely pathogenic Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 1; Fanconi anemia, complementation group S criteria provided, single submitter clinical testing
Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto RCV000496929 SCV000587497 pathogenic Hereditary breast ovarian cancer syndrome 2014-01-31 no assertion criteria provided research

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