Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584211 | SCV000689991 | likely benign | Hereditary cancer-predisposing syndrome | 2017-07-18 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002061836 | SCV002413364 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-24 | criteria provided, single submitter | clinical testing |