Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000773432 | SCV000907126 | uncertain significance | Hereditary cancer-predisposing syndrome | 2019-01-03 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000986715 | SCV001135806 | uncertain significance | Lynch syndrome 5 | 2019-05-28 | criteria provided, single submitter | clinical testing |