{{Rsnum
|rsid=4745661
|Chromosome=9
|position=77705449
|Orientation=plus
|GMAF=0.4086
|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 | 6.2 | 43.1 | 50.8
| HCB | 28.9 | 55.6 | 15.6
| JPT | 18.2 | 47.7 | 34.1
| YRI | 25.4 | 42.9 | 31.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 28.9 | 55.6 | 15.6
| 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=3E-6
  |OR=.16
  |ORtxt=[0.094-0.23] unit decrease
  |OA=1
}}