{{Rsnum
|rsid=10852453
|Chromosome=16
|position=53039876
|Orientation=plus
|GMAF=0.4164
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 26.7 | 50.0 | 23.3
| HCB | 48.8 | 44.2 | 7.0
| JPT | 42.9 | 52.4 | 4.8
| YRI | 39.3 | 50.8 | 9.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 48.8 | 44.2 | 7.0
| 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=T
  |Pval=1E-6
  |OR=.15
  |ORtxt=[0.088-0.205] unit decrease
  |OA=1
}}