{{Rsnum
|rsid=9900213
|Gene=STAT5B
|Chromosome=17
|position=42223863
|Orientation=plus
|GMAF=0.2828
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=STAT5B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 74.3 | 23.9 | 1.8
| HCB | 59.1 | 34.3 | 6.6
| JPT | 49.6 | 41.6 | 8.8
| YRI | 9.5 | 47.6 | 42.9
| ASW | 28.1 | 47.4 | 24.6
| CHB | 59.1 | 34.3 | 6.6
| CHD | 49.5 | 43.1 | 7.3
| GIH | 48.5 | 42.6 | 8.9
| LWK | 10.9 | 46.4 | 42.7
| MEX | 81.0 | 19.0 | 0.0
| MKK | 27.6 | 44.9 | 27.6
| TSI | 75.5 | 20.6 | 3.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=21470284
|Title=The signal transducer and activator of transcription 5B gene polymorphism contributes to the cholesterol metabolism in Japanese children with growth hormone deficiency
}}

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

{{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}}