{{Rsnum
|rsid=10796849
|Chromosome=11
|position=69787644
|Orientation=plus
|GMAF=0.3907
|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 | 1.6 | 24.2 | 74.2
| HCB | 19.5 | 56.1 | 24.4
| JPT | 20.5 | 47.7 | 31.8
| YRI | 58.6 | 36.2 | 5.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 19.5 | 56.1 | 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=C
  |Pval=6E-6
  |OR=.61
  |ORtxt=[0.35-0.88] unit decrease
  |OA=1
}}