Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001191473 | SCV001359295 | likely benign | Hereditary cancer-predisposing syndrome | 2019-09-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003744781 | SCV004472612 | likely benign | Familial adenomatous polyposis 1 | 2023-11-25 | criteria provided, single submitter | clinical testing |