Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075492 | SCV000106488 | likely pathogenic | Lynch syndrome | 2019-06-21 | reviewed by expert panel | curation | Multifactorial likelihood analysis posterior probability 0.95-0.99 |
Clinical Genetics and Genomics, |
RCV001269638 | SCV001449763 | pathogenic | not provided | 2019-08-30 | criteria provided, single submitter | clinical testing |