{{Rsnum
|rsid=6785049
|Gene=NR1I2
|Chromosome=3
|position=119814886
|Orientation=plus
|GMAF=0.4444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NR1I2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 42.5 | 49.6 | 8.0
| HCB | 21.9 | 54.7 | 23.4
| JPT | 21.2 | 45.1 | 33.6
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 22.8 | 77.2
| CHB | 21.9 | 54.7 | 23.4
| CHD | 18.3 | 50.5 | 31.2
| GIH | 24.8 | 47.5 | 27.7
| LWK | 0.0 | 8.2 | 91.8
| MEX | 41.4 | 50.0 | 8.6
| MKK | 3.2 | 30.1 | 66.7
| TSI | 30.4 | 55.9 | 13.7
| 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=19739075
|Title=Polymorphisms in genes of the steroid receptor superfamily modify postmenopausal breast cancer risk associated with menopausal hormone therapy
}}
{{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=20836841
|Title=Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes
|OA=1
}}

{{PMID Auto
|PMID=16952547
|Title=Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis.
}}

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