Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001185609 | SCV001351860 | likely benign | Hereditary cancer-predisposing syndrome | 2019-02-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068417 | SCV002382855 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-03-24 | criteria provided, single submitter | clinical testing |