Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001179022 | SCV001343592 | likely benign | Hereditary cancer-predisposing syndrome | 2020-02-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002558897 | SCV003327819 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-03-11 | criteria provided, single submitter | clinical testing |