Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000852296 | SCV000994915 | likely pathogenic | Lynch syndrome | 2019-06-21 | reviewed by expert panel | curation | Variant causes splicing aberration & 2 MSI-H tumours |
Gene |
RCV001805907 | SCV002054069 | pathogenic | Lynch syndrome 1 | 2021-02-02 | no assertion criteria provided | literature only |