Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582999 | SCV000691118 | likely benign | Hereditary cancer-predisposing syndrome | 2017-06-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000937296 | SCV001083079 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-31 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002372 | SCV004830979 | likely benign | Lynch syndrome | 2023-09-09 | criteria provided, single submitter | clinical testing |