Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075918 | SCV000106937 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Gene |
RCV000114849 | SCV001881478 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Harris Lab, |
RCV000114849 | SCV000148744 | not provided | not provided | no assertion provided | not provided |