Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001177571 | SCV001341805 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-11-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068197 | SCV002401375 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2022-01-17 | criteria provided, single submitter | clinical testing |