Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000409204 | SCV000488155 | uncertain significance | Lynch syndrome 5 | 2016-02-19 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000409204 | SCV001135786 | likely benign | Lynch syndrome 5 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001536952 | SCV001753770 | benign | not provided | 2019-08-30 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV002267835 | SCV002552277 | likely benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing |