Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581146 | SCV000686826 | likely benign | Hereditary cancer-predisposing syndrome | 2017-09-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003767277 | SCV002336739 | likely benign | Familial adenomatous polyposis 1 | 2021-03-07 | criteria provided, single submitter | clinical testing |