Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000875557 | SCV001018001 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2023-09-21 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001190780 | SCV001358364 | likely benign | Hereditary cancer-predisposing syndrome | 2021-05-05 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV001799003 | SCV002043630 | uncertain significance | Breast and/or ovarian cancer | 2020-06-17 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV001190780 | SCV002533657 | uncertain significance | Hereditary cancer-predisposing syndrome | 2021-07-07 | criteria provided, single submitter | curation |