{{Rsnum
|rsid=2284553
|Gene=IFNGR2
|Chromosome=21
|position=33404389
|Orientation=plus
|GMAF=0.3058
|Gene_s=IFNGR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 19.5 | 49.6 | 31.0
| HCB | 23.4 | 38.0 | 38.7
| JPT | 8.8 | 30.1 | 61.1
| YRI | 0.0 | 10.2 | 89.8
| ASW | 3.5 | 17.5 | 78.9
| CHB | 23.4 | 38.0 | 38.7
| CHD | 13.8 | 52.3 | 33.9
| GIH | 12.9 | 54.5 | 32.7
| LWK | 0.0 | 9.1 | 90.9
| MEX | 15.5 | 53.4 | 31.0
| MKK | 0.0 | 28.8 | 71.2
| TSI | 16.7 | 40.2 | 43.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23128233
  |Trait=Crohn's disease
  |Title=Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
  |RiskAllele=G
  |Pval=2E-16
  |OR=1.12
  |ORtxt=[1.086-1.162]
  |OA=1
}}

{{PMID Auto
|PMID=20980339
|Title=Hepatitis B viraemia: its heritability and association with common genetic variation in the interferon gamma signalling pathway.
}}

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