Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001188844 | SCV001355990 | likely benign | Hereditary cancer-predisposing syndrome | 2018-12-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003538593 | SCV003272454 | likely benign | Familial adenomatous polyposis 1 | 2023-12-04 | criteria provided, single submitter | clinical testing |