{{Rsnum
|rsid=12460587
|Chromosome=19
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ZNF841
|position=52083666
|Gene_s=ZNF841
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 3.5 | 29.2 | 67.3
| HCB | 15.6 | 41.5 | 43.0
| JPT | 13.3 | 44.2 | 42.5
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 10.5 | 89.5
| CHB | 15.6 | 41.5 | 43.0
| CHD | 14.0 | 48.6 | 37.4
| GIH | 4.0 | 47.5 | 48.5
| LWK | 0.9 | 14.5 | 84.5
| MEX | 8.6 | 36.2 | 55.2
| MKK | 0.0 | 16.0 | 84.0
| TSI | 4.9 | 30.4 | 64.7
| 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=G
  |Pval=2E-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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}