Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581264 | SCV000690049 | likely benign | Hereditary cancer-predisposing syndrome | 2017-04-24 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002065091 | SCV002494016 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-12 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV000581264 | SCV002534449 | likely benign | Hereditary cancer-predisposing syndrome | 2021-02-09 | criteria provided, single submitter | curation | |
All of Us Research Program, |
RCV004002333 | SCV004827851 | likely benign | Lynch syndrome | 2023-08-15 | criteria provided, single submitter | clinical testing |