Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001187719 | SCV001354589 | likely benign | Hereditary cancer-predisposing syndrome | 2019-01-31 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003744772 | SCV003324074 | likely benign | Familial adenomatous polyposis 1 | 2022-10-15 | criteria provided, single submitter | clinical testing |