Annotation Detail
Information
- Associated Genes
- PTPN22
- Associated Variants
-
PTPN22 MUTATION
PTPN22 MUTATION - Associated Disease
- rheumatoid arthritis
- Source Database
- DisGeNET
- Description
- A C-to-T single-nucleotide polymorphism (SNP) located at position 1858 of human protein tyrosine phosphatase PTPN22 complementary DNA carries the highest risk of rheumatoid arthritis (RA) among all non-HLA genetic variants.
- Pubmed
- 26019128
- Section of the abstract supporting the evidence
- OBJECTIVE
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 1
- Original source reporting the Gene Disease association
- BeFree,CTD_human,GAD,GWASCAT,LHGDN,UNIPROT
- DisGENET score for the Gene Disease association
- 0.524345610778177
Drugs