Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001186990 | SCV001353645 | likely benign | Hereditary cancer-predisposing syndrome | 2018-11-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068450 | SCV002353676 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-12-15 | criteria provided, single submitter | clinical testing |