Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000076783 | SCV000108271 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Gene |
RCV001540228 | SCV001758088 | benign | not provided | 2018-12-06 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001540228 | SCV002058087 | benign | not provided | 2023-11-30 | criteria provided, single submitter | clinical testing |