Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001696861 | SCV000569364 | likely benign | not provided | 2019-03-11 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000579813 | SCV000685362 | likely benign | Hereditary cancer-predisposing syndrome | 2016-07-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002056774 | SCV002359366 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-09-25 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004003327 | SCV004832507 | likely benign | Lynch syndrome | 2023-10-23 | criteria provided, single submitter | clinical testing |