Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001184858 | SCV001350944 | likely benign | Hereditary cancer-predisposing syndrome | 2018-12-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068396 | SCV002413720 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-09-01 | criteria provided, single submitter | clinical testing |