Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075153 | SCV000106143 | pathogenic | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | Coding sequence variation resulting in a stop codon |
Department of Pathology and Laboratory Medicine, |
RCV001355070 | SCV001549838 | uncertain significance | not provided | no assertion criteria provided | clinical testing |