Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001182380 | SCV001347815 | likely benign | Hereditary cancer-predisposing syndrome | 2019-03-19 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068316 | SCV002484943 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2020-12-23 | criteria provided, single submitter | clinical testing |