Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000777573 | SCV000913436 | likely benign | Hereditary cancer-predisposing syndrome | 2018-02-16 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002535624 | SCV003322497 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-02-21 | criteria provided, single submitter | clinical testing |