Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001180419 | SCV001345347 | likely benign | Hereditary cancer-predisposing syndrome | 2022-01-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002560801 | SCV003238858 | benign | Hereditary nonpolyposis colorectal neoplasms | 2023-07-10 | criteria provided, single submitter | clinical testing |