{{Rsnum
|rsid=12188164
|Gene=AHRR
|Chromosome=5
|position=428121
|Orientation=plus
|GMAF=0.1878
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=AHRR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 18.8 | 46.4 | 34.8
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 12.3 | 87.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 6.9 | 35.6 | 57.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 8.6 | 39.7 | 51.7
| MKK | 0.0 | 0.6 | 99.4
| TSI | 2.9 | 43.1 | 53.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21602797
|Trait=None
|Title=Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
|RiskAllele=A
|Pval=0.000004
|OR=None
|ORtxt=None
|OA=1
}}

{{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}}