Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001190559 | SCV001358067 | likely benign | Hereditary cancer-predisposing syndrome | 2019-07-08 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003614083 | SCV004446239 | likely benign | Familial adenomatous polyposis 2 | 2023-03-16 | criteria provided, single submitter | clinical testing |