Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001178648 | SCV001343157 | uncertain significance | Hereditary cancer-predisposing syndrome | 2019-01-10 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003537497 | SCV002492422 | likely benign | Familial adenomatous polyposis 1 | 2024-01-10 | criteria provided, single submitter | clinical testing |