{{Rsnum
|rsid=1598106
|Chromosome=2
|position=13889623
|Orientation=minus
|GMAF=0.3522
|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 | 30.8 | 52.3 | 16.9
| HCB | 64.4 | 31.1 | 4.4
| JPT | 71.1 | 24.4 | 4.4
| YRI | 31.1 | 47.5 | 21.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 64.4 | 31.1 | 4.4
| 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=2E-7
  |OR=.16
  |ORtxt=[0.1-0.23] unit decrease
  |OA=1
}}