Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582267 | SCV000690253 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000944019 | SCV001089979 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2019-10-19 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002347 | SCV004842038 | likely benign | Lynch syndrome | 2023-08-15 | criteria provided, single submitter | clinical testing |