Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581728 | SCV000691057 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002061905 | SCV002340219 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-06-02 | criteria provided, single submitter | clinical testing |