Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000775370 | SCV000909681 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-10-07 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001856113 | SCV002238032 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-11-17 | criteria provided, single submitter | clinical testing |