{{Rsnum
|rsid=3814057
|Gene=NR1I2
|Chromosome=3
|position=119818407
|Orientation=plus
|GMAF=0.3255
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=NR1I2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 82.3 | 16.8 | 0.9
| HCB | 30.3 | 57.6 | 12.1
| JPT | 20.5 | 54.5 | 25.0
| YRI | 21.3 | 59.6 | 19.1
| ASW | 30.9 | 50.9 | 18.2
| CHB | 30.3 | 57.6 | 12.1
| CHD | 26.4 | 53.8 | 19.8
| GIH | 55.0 | 35.0 | 10.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 66.7 | 31.6 | 1.8
| MKK | 30.7 | 58.8 | 10.5
| TSI | 71.3 | 25.7 | 3.0
| 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
}}

{{PMID Auto
|PMID=21830270
|Title=Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease.
}}

{{PMID Auto
|PMID=21954916
|Title=Variants of the human NR1I2 (PXR) locus in chronic periodontitis.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}