Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581980 | SCV000691100 | likely benign | Hereditary cancer-predisposing syndrome | 2015-07-21 | criteria provided, single submitter | clinical testing | |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV000985914 | SCV001134608 | uncertain significance | not provided | 2019-05-28 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002369 | SCV004815151 | uncertain significance | Lynch syndrome | 2023-04-03 | criteria provided, single submitter | clinical testing |