Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581809 | SCV000690144 | benign | Hereditary cancer-predisposing syndrome | 2017-06-26 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV000581809 | SCV002526771 | likely benign | Hereditary cancer-predisposing syndrome | 2021-01-31 | criteria provided, single submitter | curation | |
Center for Genomic Medicine, |
RCV003320711 | SCV004025233 | likely benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002337 | SCV004824938 | benign | Lynch syndrome | 2023-09-04 | criteria provided, single submitter | clinical testing |