Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Evidence- |
RCV000661068 | SCV000783315 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2017-12-15 | reviewed by expert panel | curation | Variant allele predicted to encode a truncated non-functional protein. |
Department of Pathology and Molecular Medicine, |
RCV000496614 | SCV000588060 | pathogenic | Hereditary breast ovarian cancer syndrome | 2017-04-20 | criteria provided, single submitter | clinical testing |