Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000074979 | SCV000108194 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Mendelics | RCV000986751 | SCV001135866 | benign | Lynch syndrome 5 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001618243 | SCV001845720 | benign | not provided | 2019-08-13 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV002267834 | SCV002552380 | likely benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing | |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV001618243 | SCV004222032 | benign | not provided | 2023-05-16 | criteria provided, single submitter | clinical testing |