Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000776168 | SCV000911252 | likely benign | Hereditary cancer-predisposing syndrome | 2018-06-18 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003768398 | SCV002419878 | likely benign | Familial adenomatous polyposis 1 | 2024-01-21 | criteria provided, single submitter | clinical testing |