Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584519 | SCV000689851 | likely benign | Hereditary cancer-predisposing syndrome | 2016-07-18 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002061823 | SCV002472226 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2021-06-08 | criteria provided, single submitter | clinical testing |