Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000557738 | SCV000633567 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2024-01-17 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001712768 | SCV000721964 | likely benign | not provided | 2023-03-07 | criteria provided, single submitter | clinical testing | See Variant Classification Assertion Criteria. |
Color Diagnostics, |
RCV001184256 | SCV001350201 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-27 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV003492092 | SCV004240387 | uncertain significance | Breast and/or ovarian cancer | 2023-04-25 | criteria provided, single submitter | clinical testing |