Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001175713 | SCV001339422 | likely benign | Hereditary cancer-predisposing syndrome | 2018-12-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003769863 | SCV002940434 | likely benign | Familial adenomatous polyposis 1 | 2022-04-17 | criteria provided, single submitter | clinical testing |