{{Rsnum
|rsid=2069718
|Gene=IFNG
|Chromosome=12
|position=68156382
|Orientation=minus
|GMAF=0.3834
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IFNG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 55.8 | 14.2
| HCB | 2.9 | 21.2 | 75.9
| JPT | 0.0 | 14.2 | 85.8
| YRI | 12.9 | 45.6 | 41.5
| ASW | 14.0 | 49.1 | 36.8
| CHB | 2.9 | 21.2 | 75.9
| CHD | 0.9 | 24.8 | 74.3
| GIH | 27.7 | 51.5 | 20.8
| LWK | 15.5 | 47.3 | 37.3
| MEX | 10.3 | 50.0 | 39.7
| MKK | 26.3 | 49.4 | 24.4
| TSI | 47.1 | 45.1 | 7.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=19919944
|Title=Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus
}}

{{PMID|15570643}} Epistatic interactions between HLA-DRB1 and interleukin 4, but not interferon-gamma, increase susceptibility to giant cell arteritis.

{{PMID|17215375|OA=1
}} A functional SNP of interferon-gamma gene is important for interferon-alpha-induced and spontaneous recovery from hepatitis C virus infection.

{{PMID|18385742}} A single nucleotide polymorphism (A --> G) in intron 3 of IFNgamma gene is associated with asthma.

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

{{PMID|20196868|OA=1
}} Polymorphisms in IL-1beta, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis.

{{PMID Auto
|PMID=23737189
|Title=IFNG polymorphisms are associated with tuberculosis in Han Chinese pediatric female population
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}