Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075828 | SCV000106841 | pathogenic | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | Coding sequence variation introducing premature termination codon |
Department of Pathology and Laboratory Medicine, |
RCV000075828 | SCV000592330 | pathogenic | Lynch syndrome | 2013-08-20 | criteria provided, single submitter | clinical testing |