{{Rsnum
|rsid=12721613
|Gene=NR1I2
|Chromosome=3
|position=119807329
|Orientation=plus
|GMAF=0.03719
|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 | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 63.9 | 33.3 | 2.7
| ASW | 78.9 | 21.1 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 69.1 | 30.0 | 0.9
| MEX | 98.3 | 1.7 | 0.0
| MKK | 83.9 | 14.8 | 1.3
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs12721613
|Name_s=g.79C>T; Pro27Ser
|Gene_s=NR1I2
|Feature=Exon/NonSyn
|Evidence=PubMed ID:17050801
|Annotation=study of 54 livers; variant not associated with altered midazolam clearance
|Drugs=midazolam
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA165363643
}}

{{PharmGKB
|RSID=rs12721613
|Name_s=P27S
|Gene_s=NR1I2
|Feature=Exon/NonSyn
|Evidence=PubMed ID:11602521
|Annotation=cell based studies; transcription and induction same as WT
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA165363576
}}

{{GET Evidence
|gene=NR1I2
|aa_change=Pro66Ser
|aa_change_short=P66S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12721613
|overall_frequency_n=483
|overall_frequency_d=10758
|overall_frequency=0.0448968
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}