Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000777580 | SCV000913443 | likely benign | Hereditary cancer-predisposing syndrome | 2018-02-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003535848 | SCV001632864 | likely benign | Familial adenomatous polyposis 1 | 2023-05-17 | criteria provided, single submitter | clinical testing |