Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001177737 | SCV001342000 | likely benign | Hereditary cancer-predisposing syndrome | 2019-01-30 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002555478 | SCV003513506 | likely benign | Familial adenomatous polyposis 2 | 2023-06-09 | criteria provided, single submitter | clinical testing |