{{Rsnum
|rsid=33996649
|Gene=PTPN22
|Chromosome=1
|position=113852067
|Orientation=plus
|GMAF=0.0124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PTPN22,RP5-1073O3.2
}}{{omim
|desc=PROTEIN TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 22; PTPN22
|id=600716
|rsnum=33996649
}}

{{PMID Auto
|PMID=21131644
|Title=Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis
|OA=1
}}

{{PMID Auto
|PMID=21287672
|Title=Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis
}}

{{omim
|id=152700
|rsnum=33996649
}}

{{PMID|16175503|OA=1
}} PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

{{PMID|21193990}} A PTPN22 promoter polymorphism -1123G>C is associated with RA pathogenesis in Chinese.

{{PMID|21279993}} The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples.

{{GET Evidence
|gene=PTPN22
|aa_change=Arg263Gln
|aa_change_short=R263Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs33996649
|overall_frequency_n=176
|overall_frequency_d=10758
|overall_frequency=0.0163599
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23450494
|Title=[Association of polymorphisms of PTPN22 and PADI4 genes with rheumatoid arthritis in Yunnan]
}}

{{PMID Auto
|PMID=23946333
|Title=Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis
}}

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