{{Rsnum
|rsid=3814055
|Gene=NR1I2
|Chromosome=3
|position=119781188
|Orientation=plus
|GMAF=0.3242
|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 | 44.2 | 44.2 | 11.5
| HCB | 54.0 | 39.4 | 6.6
| JPT | 54.5 | 36.6 | 8.9
| YRI | 57.1 | 32.7 | 10.2
| ASW | 45.6 | 45.6 | 8.8
| CHB | 54.0 | 39.4 | 6.6
| CHD | 62.4 | 31.2 | 6.4
| GIH | 33.7 | 50.5 | 15.8
| LWK | 50.9 | 38.2 | 10.9
| MEX | 41.4 | 55.2 | 3.4
| MKK | 58.1 | 39.4 | 2.6
| TSI | 37.3 | 50.0 | 12.7
| 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=20218903
|Title=Genetic polymorphisms of CYP1A2, CYP3A4, CYP3A5, pregnane/steroid X receptor and constitutive androstane receptor in 207 healthy Spanish volunteers
}}

{{PMID Auto
|PMID=17828778
|Title=Role of the PXR gene locus in inflammatory bowel diseases.
}}

{{PMID Auto
|PMID=20222094
|Title=A role for the pregnane X receptor in flucloxacillin-induced liver injury.
}}

{{PMID Auto
|PMID=20354687
|Title=Explaining variability in ciclosporin exposure in adult kidney transplant recipients.
|OA=1
}}

{{PMID Auto
|PMID=21245992
|Title=Polymorphisms in NF-kappaB, PXR, LXR, PPARgamma and risk of inflammatory bowel disease.
|OA=1
}}

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