{{Rsnum
|rsid=6503695
|Gene=STAT3
|Chromosome=17
|position=42347515
|Orientation=plus
|GMAF=0.3315
|Gene_s=STAT3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 13.3 | 41.6 | 45.1
| HCB | 12.4 | 43.8 | 43.8
| JPT | 14.2 | 48.7 | 37.2
| YRI | 17.7 | 46.3 | 36.1
| ASW | 10.5 | 50.9 | 38.6
| CHB | 12.4 | 43.8 | 43.8
| CHD | 12.8 | 52.3 | 34.9
| GIH | 15.8 | 42.6 | 41.6
| LWK | 12.7 | 47.3 | 40.0
| MEX | 0.0 | 39.7 | 60.3
| MKK | 25.6 | 43.6 | 30.8
| TSI | 11.8 | 42.2 | 46.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=22205606
|Title=JAK2 and STAT3 polymorphisms in a Han Chinese Population with Behcet's disease
}}

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

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

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

{{PMID|20065083|OA=1
}} A polymorphism associated with STAT3 expression and response of chronic myeloid leukemia to interferon alpha.

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

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

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

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}