Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075866 | SCV000106883 | likely pathogenic | Lynch syndrome | 2019-06-21 | reviewed by expert panel | curation | Variant causes splicing aberration & 2 MSI-H tumours. |