Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001403319 | SCV001605186 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2018-11-28 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004003286 | SCV004825347 | likely benign | Lynch syndrome | 2023-05-04 | criteria provided, single submitter | clinical testing |