Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001184869 | SCV001350956 | likely benign | Hereditary cancer-predisposing syndrome | 2019-02-04 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002559876 | SCV003321139 | likely benign | Peutz-Jeghers syndrome | 2023-09-10 | criteria provided, single submitter | clinical testing |