{{Rsnum
|rsid=1310182
|Gene=PTPN22
|Chromosome=1
|position=113830881
|Orientation=minus
|GMAF=0.4614
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PTPN22,RP5-1073O3.2
}}{{PMID Auto
|PMID=20510318
|Title=Association of PTPN22 Haplotypes with Type 1 Diabetes in the Japanese Population
}}

{{PMID Auto
|PMID=20615141
|Title=Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population
}}

{{PMID|16175503|OA=1
}} 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|OA=1
}} Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.

{{PMID|18466461|OA=1
}} Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.

{{PMID|18466529|OA=1
}} Comparing strategies for evaluation of candidate genes in case-control studies using family data.

{{PMID|18466531|OA=1
}} Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.

{{PMID|18466575|OA=1
}} 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|OA=1
}} No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations.

{{PMID Auto
|PMID=25073032
|Title=Association Between a Gain-of-Function Variant of PTPN22 and Rejection in Liver Transplantation
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}