Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001187052 | SCV001353711 | likely benign | Hereditary cancer-predisposing syndrome | 2019-07-16 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003744770 | SCV003206449 | likely benign | Familial adenomatous polyposis 1 | 2023-06-29 | criteria provided, single submitter | clinical testing |