{{Rsnum
|rsid=7137515
|Chromosome=12
|position=82068447
|Orientation=plus
|GMAF=0.3595
|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 | 50.8 | 32.3 | 16.9
| HCB | 55.6 | 42.2 | 2.2
| JPT | 60.0 | 35.6 | 4.4
| YRI | 23.8 | 46.0 | 30.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 55.6 | 42.2 | 2.2
| 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=6E-6
  |OR=.16
  |ORtxt=[0.093-0.235] unit decrease
  |OA=1
}}