Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000702198 | SCV000831042 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-08-23 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001189491 | SCV001356799 | likely benign | Hereditary cancer-predisposing syndrome | 2019-05-31 | criteria provided, single submitter | clinical testing |