{{Rsnum
|rsid=2126200
|Chromosome=11
|position=123002368
|Orientation=plus
|GMAF=0.4867
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 21.9 | 59.4 | 18.8
| HCB | 35.6 | 55.6 | 8.9
| JPT | 25.0 | 40.9 | 34.1
| YRI | 23.8 | 36.5 | 39.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.6 | 55.6 | 8.9
| 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=C
  |Pval=7E-6
  |OR=.14
  |ORtxt=[0.078-0.2] unit decrease
  |OA=1
}}