Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000074980 | SCV000108195 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV003477464 | SCV004222033 | benign | not provided | 2023-08-11 | criteria provided, single submitter | clinical testing |