{{Rsnum
|rsid=2293152
|Gene=STAT3
|Chromosome=17
|position=42329511
|Orientation=minus
|GMAF=0.3792
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=STAT3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 12.7 | 50.8 | 36.5
| HCB | 31.1 | 53.3 | 15.6
| JPT | 11.4 | 40.9 | 47.7
| YRI | 0.0 | 17.7 | 82.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 31.1 | 53.3 | 15.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19653082
|Title=Strong Evidence of a Combination Polymorphism of the Tyrosine Kinase 2 Gene and the Signal Transducer and Activator of Transcription 3 Gene as a DNA-Based Biomarker for Susceptibility to Crohn's Disease in the Japanese Population
|OA=1
}}

{{PMID Auto
|PMID=19776189
|Title=Dietary saturated fat modulates the association between STAT3 polymorphisms and abdominal obesity in adults
}}

{{PMID Auto
|PMID=22205606
|Title=JAK2 and STAT3 polymorphisms in a Han Chinese Population with Behcet's disease
}}

{{PMID Auto GWAS
|PMID=22190364
|Trait=None
|Title=Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
|RiskAllele=C
|Pval=4E-8
|OR=1.2200
|ORtxt=None
|OA=1
}}
{{PMID Auto
|PMID=15935090
|Title=Polymorphisms in signal transducer and activator of transcription 3 and lung function in asthma.
|OA=1
}}

{{PMID Auto
|PMID=17636079
|Title=Common STAT3 variants are not associated with obesity or insulin resistance in female twins.
|OA=1
}}

{{PMID Auto
|PMID=18451776
|Title=Study of genetic variation in the STAT3 on obesity and insulin resistance in male adults.
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|OA=1
}}

{{PMID Auto
|PMID=18789715
|Title=Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease.
}}

{{PMID Auto
|PMID=20159113
|Title=Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
|OA=1
}}

{{PMID Auto
|PMID=21068102
|Title=Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese.
}}

{{PMID Auto
|PMID=21310444
|Title=Mitochondrial DNA copy number is modulated by genetic variation in the signal transducer and activator of transcription 3 (STAT3).
}}

{{PMID Auto
|PMID=22095036
|Title=Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample.
}}

{{PMID Auto
|PMID=23127549
|Title=Influence of the STAT3 genetic variants in the susceptibility to psoriatic arthritis and Behcet's disease
}}

{{PMID Auto
|PMID=23611997
|Title=JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population
}}

{{PMID Auto
|PMID=24081513
|Title=Association of single-nucleotide polymorphisms in the STAT3 gene with autoimmune thyroid disease in Chinese individuals
|OA=1
}}

{{PMID Auto
|PMID=24781989
|Title=Association between STAT3 gene polymorphisms and ulcerative colitis susceptibility: a case-control study in the Chinese Han population
}}

{{PMID Auto
|PMID=24864251
|Title=rs744166 Polymorphism of the STAT3 Gene Is Associated with Risk of Gastric Cancer in a Chinese Population
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}