Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001176254 | SCV001340146 | likely benign | Hereditary cancer-predisposing syndrome | 2020-01-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002067877 | SCV002440821 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-06-20 | criteria provided, single submitter | clinical testing |