[PMID 20510318] Association of PTPN22 Haplotypes with Type 1 Diabetes in the Japanese Population


[PMID 20615141] Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population

[PMID 16175503] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

[PMID 17934143] Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.

[PMID 18341666] Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.

[PMID 18466461] Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.

[PMID 18466529] Comparing strategies for evaluation of candidate genes in case-control studies using family data.

[PMID 18466531] Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.

[PMID 18466575] Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis.

[PMID 21193990] A PTPN22 promoter polymorphism -1123G>C is associated with RA pathogenesis in Chinese.

[PMID 22396730] No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations.


[PMID 25073032] Association Between a Gain-of-Function Variant of PTPN22 and Rejection in Liver Transplantation

rs1310182

Parent Gene: PTPN22

Importance: 1
Less common allele: A = 49%
More common allele: G = 51%
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