{{Rsnum
|rsid=11666341
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=52098146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 31.9 | 65.5
| HCB | 22.6 | 44.4 | 33.1
| JPT | 21.6 | 49.5 | 28.8
| YRI | 1.4 | 20.4 | 78.2
| ASW | 3.5 | 22.8 | 73.7
| CHB | 22.6 | 44.4 | 33.1
| CHD | 19.3 | 51.4 | 29.4
| GIH | 5.0 | 46.0 | 49.0
| LWK | 3.7 | 18.3 | 78.0
| MEX | 5.2 | 44.8 | 50.0
| MKK | 0.0 | 22.1 | 77.9
| TSI | 5.0 | 30.7 | 64.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24280104
  |Trait=Bronchodilator response in asthma (inhaled corticosteroid treatment interaction)
  |Title=Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics.
  |RiskAllele=A
  |Pval=1E-9
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}