{{Rsnum
|rsid=300032
|Chromosome=16
|position=86647390
|Orientation=plus
|GMAF=0.3301
|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 | 79.4 | 19.0 | 1.6
| HCB | 20.5 | 65.9 | 13.6
| JPT | 35.6 | 46.7 | 17.8
| YRI | 21.0 | 46.8 | 32.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 20.5 | 65.9 | 13.6
| 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-7
  |OR=.23
  |ORtxt=[0.14-0.32] unit increase
  |OA=1
}}