Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001178218 | SCV001342598 | likely benign | Hereditary cancer-predisposing syndrome | 2018-12-10 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001427494 | SCV001630177 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-08-09 | criteria provided, single submitter | clinical testing |