{{Rsnum
|rsid=1554286
|Gene=IL10
|Chromosome=1
|position=206770888
|Orientation=minus
|GMAF=0.3811
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IL10
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 69.0 | 27.4 | 3.5
| HCB | 9.5 | 37.2 | 53.3
| JPT | 8.8 | 52.2 | 38.9
| YRI | 27.9 | 49.7 | 22.4
| ASW | 42.1 | 43.9 | 14.0
| CHB | 9.5 | 37.2 | 53.3
| CHD | 6.4 | 53.2 | 40.4
| GIH | 40.6 | 45.5 | 13.9
| LWK | 34.5 | 54.5 | 10.9
| MEX | 39.7 | 48.3 | 12.1
| MKK | 37.8 | 50.0 | 12.2
| TSI | 63.7 | 33.3 | 2.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=20804371
|Title=Association between Single-Nucleotide Polymorphisms in Mal/TIRAP and Interleukin-10 Genes and Susceptibility to Invasive Haemophilus influenzae Serotype b Infection in Immunized Children
}}

{{PMID Auto
|PMID=21917900
|Title=Genetic Variations and Interactions in Anti-inflammatory Cytokine Pathway Genes in the Outcome of Leprosy: A Study Conducted on a MassARRAY Platform
}}

{{PMID|16672419|OA=1
}} Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation.

{{PMID|17690160|OA=1
}} Raised interleukin-10 is an indicator of poor outcome and enhanced systemic inflammation in patients with acute coronary syndrome.

{{PMID|18426996|OA=1
}} Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.

{{PMID|18479293|OA=1
}} Evaluation of IL10, IL19 and IL20 gene polymorphisms and chronic hepatitis B infection outcome.

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

{{PMID|18640487|OA=1
}} Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.

{{PMID|19468064|OA=1
}} Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.

{{PMID|19503741|OA=1
}} Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

{{PMID|19505919|OA=1
}} Toll-like receptor signaling pathway variants and prostate cancer mortality.

{{PMID|19753309|OA=1
}} SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

{{PMID|19907653|OA=1
}} Selection for genetic variation inducing pro-inflammatory responses under adverse environmental conditions in a Ghanaian population.

{{PMID|20416077|OA=1
}} Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

{{PMID|20525402|OA=1
}} Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study.

{{PMID|20617178|OA=1
}} Leprosy and the adaptation of human toll-like receptor 1.

{{PMID|20622879}} Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci.

{{PMID|21532858|OA=1
}} Association of IL10, IL10RA, and IL10RB polymorphisms with benign prostate hyperplasia in Korean population.

{{PMID|22378604}} Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behcet's disease.

{{PMID Auto
|PMID=24040186
|Title=Relationship of serum interleukin-10 and its genetic variations with ischemic stroke in a chinese general population
|OA=1
}}

{{PMID Auto
|PMID=23096091
|Title=Association between IL10, IL10RA, and IL10RB SNPs and ischemic stroke with hypertension in Korean population.
}}

{{PMID Auto
|PMID=24903972
|Title=Genetic predisposition to calcific aortic stenosis and mitral annular calcification
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}