Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001177037 | SCV001341150 | likely benign | Hereditary cancer-predisposing syndrome | 2019-11-19 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004006354 | SCV004818722 | likely benign | Lynch syndrome | 2023-03-23 | criteria provided, single submitter | clinical testing |