Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583960 | SCV000691076 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002061908 | SCV002329642 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2021-11-07 | criteria provided, single submitter | clinical testing |