Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001432016 | SCV001634780 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-11-01 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004006985 | SCV004836810 | likely benign | Lynch syndrome | 2023-10-02 | criteria provided, single submitter | clinical testing |