Annotation Detail
Information
- Associated Genes
- MSH6
- Associated Variants
-
MSH6 MUTATION
MSH6 MUTATION - Associated Disease
- Hereditary Nonpolyposis Colorectal Cancer
- Source Database
- DisGeNET
- Description
- Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.
- Pubmed
- 25318681
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree,CLINVAR,GAD,ORPHANET
- DisGENET score for the Gene Disease association
- 0.277111591604881
Drugs