Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001185389 | SCV001351585 | likely benign | Hereditary cancer-predisposing syndrome | 2019-06-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068413 | SCV002360044 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-01-26 | criteria provided, single submitter | clinical testing |