Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075340 | SCV000106326 | pathogenic | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | In-frame large deletion interrupting funtional domains |
Department of Pathology and Laboratory Medicine, |
RCV000075340 | SCV000590986 | pathogenic | Lynch syndrome | criteria provided, single submitter | clinical testing | ||
Mayo Clinic Laboratories, |
RCV000202163 | SCV000257062 | pathogenic | not provided | no assertion criteria provided | research |