Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001185775 | SCV001352056 | likely benign | Hereditary cancer-predisposing syndrome | 2018-12-17 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001434669 | SCV001637480 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-09-23 | criteria provided, single submitter | clinical testing |