Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001183627 | SCV001349421 | likely benign | Hereditary cancer-predisposing syndrome | 2019-06-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001394312 | SCV001595994 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2020-07-25 | criteria provided, single submitter | clinical testing |