Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001183153 | SCV001348810 | likely benign | Hereditary cancer-predisposing syndrome | 2019-09-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002559045 | SCV003474248 | likely benign | Familial adenomatous polyposis 2 | 2022-11-06 | criteria provided, single submitter | clinical testing |