Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582514 | SCV000690322 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002061852 | SCV002464797 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-02-01 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002351 | SCV004830124 | likely benign | Lynch syndrome | 2023-12-01 | criteria provided, single submitter | clinical testing |