Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001177651 | SCV001341900 | likely benign | Hereditary cancer-predisposing syndrome | 2019-01-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068201 | SCV002381698 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2021-12-11 | criteria provided, single submitter | clinical testing |