Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001804648 | SCV002053466 | likely benign | Hereditary cancer-predisposing syndrome | 2021-07-29 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002074192 | SCV002392718 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-12-22 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004009104 | SCV004828726 | likely benign | Lynch syndrome | 2023-09-17 | criteria provided, single submitter | clinical testing |