Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582906 | SCV000690156 | likely benign | Hereditary cancer-predisposing syndrome | 2016-12-09 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002341 | SCV004828529 | likely benign | Lynch syndrome | 2023-09-04 | criteria provided, single submitter | clinical testing |