Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583765 | SCV000690257 | likely benign | Hereditary cancer-predisposing syndrome | 2017-07-21 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002529254 | SCV002958431 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-04-21 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002348 | SCV004834310 | likely benign | Lynch syndrome | 2023-12-01 | criteria provided, single submitter | clinical testing |