{{Rsnum
|rsid=12488820
|Gene=NR1I2
|Chromosome=3
|position=119783222
|Orientation=plus
|GMAF=0.4807
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NR1I2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 41.6 | 46.0 | 12.4
| HCB | 54.0 | 39.4 | 6.6
| JPT | 54.5 | 36.6 | 8.9
| YRI | 1.4 | 13.6 | 85.0
| ASW | 0.0 | 22.8 | 77.2
| CHB | 54.0 | 39.4 | 6.6
| CHD | 62.4 | 31.2 | 6.4
| GIH | 20.8 | 55.4 | 23.8
| LWK | 0.0 | 12.7 | 87.3
| MEX | 32.8 | 62.1 | 5.2
| MKK | 1.3 | 37.8 | 60.9
| TSI | 36.3 | 45.1 | 18.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=19940802
|Title=The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver disease
}}

{{PMID Auto
|PMID=19958310
|Title=The influence of common gene variants of the xenobiotic receptor (PXR) in genetic susceptibility to intrahepatic cholestasis of pregnancy
}}

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