Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001189082 | SCV001356286 | likely benign | Hereditary cancer-predisposing syndrome | 2019-12-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001443671 | SCV001646655 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-06-17 | criteria provided, single submitter | clinical testing |