{{Rsnum
|rsid=1523127
|Gene=NR1I2
|Chromosome=3
|position=119782192
|Orientation=minus
|GMAF=0.4578
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=NR1I2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 11.5 | 44.2 | 44.2
| HCB | 6.6 | 39.7 | 53.7
| JPT | 8.8 | 37.2 | 54.0
| YRI | 74.1 | 23.8 | 2.0
| ASW | 63.2 | 29.8 | 7.0
| CHB | 6.6 | 39.7 | 53.7
| CHD | 6.4 | 31.2 | 62.4
| GIH | 19.8 | 53.5 | 26.7
| LWK | 81.5 | 17.6 | 0.9
| MEX | 3.4 | 58.6 | 37.9
| MKK | 52.9 | 40.0 | 7.1
| TSI | 12.9 | 49.5 | 37.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=20836841
|Title=Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes
|OA=1
}}

Gene variants associated with [[deep vein thrombosis]].{{PMID|18349091}}

Updated analysis of gene variants associated with [[deep vein thrombosis]].{{PMID|20124536}}

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

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

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

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

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