{{Rsnum
|rsid=12721607
|Gene=NR1I2
|Chromosome=3
|position=119807356
|Orientation=plus
|GMAF=0.005969
|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 | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 1.7 | 98.3
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs12721607
|Name_s=G36R
|Gene_s=NR1I2
|Feature=Exon/NonSyn
|Evidence=PubMed ID:11602521
|Annotation=cell based studies; increased induction w/ corticosterone
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA165363574
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}