{{Rsnum
|rsid=1853639
|Gene=KRT18P42
|Chromosome=6
|position=86897124
|Orientation=plus
|GMAF=0.3733
|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 | 43.1 | 36.9 | 20.0
| HCB | 35.6 | 40.0 | 24.4
| JPT | 20.9 | 53.5 | 25.6
| YRI | 41.3 | 44.4 | 14.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.6 | 40.0 | 24.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=8E-6
  |OR=.18
  |ORtxt=[0.099-0.254] unit decrease
  |OA=1
}}