Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581379 | SCV000688011 | likely benign | Hereditary cancer-predisposing syndrome | 2016-06-30 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000869942 | SCV001011404 | likely benign | BAP1-related tumor predisposition syndrome | 2023-12-08 | criteria provided, single submitter | clinical testing |