Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584344 | SCV000689811 | likely benign | Hereditary cancer-predisposing syndrome | 2017-05-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001489213 | SCV001693750 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-12-31 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002322 | SCV004840843 | likely benign | Lynch syndrome | 2023-12-18 | criteria provided, single submitter | clinical testing |