Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001188981 | SCV001356173 | likely benign | Hereditary cancer-predisposing syndrome | 2018-11-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002069052 | SCV002370995 | likely benign | Familial adenomatous polyposis 2 | 2020-11-23 | criteria provided, single submitter | clinical testing |