Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001457998 | SCV001661813 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2020-06-06 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004007070 | SCV004837112 | likely benign | Lynch syndrome | 2024-02-05 | criteria provided, single submitter | clinical testing |