{{Rsnum
|rsid=2080501
|Gene=ZNF423
|Chromosome=16
|position=49609655
|Orientation=plus
|GMAF=0.4311
|Gene_s=ZNF423
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.0 | 51.3 | 25.7
| HCB | 27.7 | 43.8 | 28.5
| JPT | 28.6 | 57.1 | 14.3
| YRI | 92.5 | 7.5 | 0.0
| ASW | 80.7 | 10.5 | 8.8
| CHB | 27.7 | 43.8 | 28.5
| CHD | 24.1 | 46.3 | 29.6
| GIH | 31.7 | 52.5 | 15.8
| LWK | 72.7 | 26.4 | 0.9
| MEX | 12.1 | 58.6 | 29.3
| MKK | 42.3 | 46.8 | 10.9
| TSI | 20.6 | 46.1 | 33.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=G
  |Pval=4E-6
  |OR=.14
  |ORtxt=[0.082-0.203] unit increase
  |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}}