{{Rsnum
|rsid=4821897
|Chromosome=22
|position=39439582
|Orientation=plus
|GMAF=0.1841
|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 | 8.0 | 37.2 | 54.9
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 7.5 | 31.5 | 61.0
| ASW | 1.8 | 36.8 | 61.4
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 1.0 | 15.8 | 83.2
| LWK | 6.4 | 48.2 | 45.5
| MEX | 0.0 | 22.4 | 77.6
| MKK | 5.1 | 45.5 | 49.4
| TSI | 11.8 | 46.1 | 42.2
| 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=4E-18
  |OR=.30
  |ORtxt=[0.23-0.36] unit decrease
  |OA=1
}}

{{on chip | Illumina Human 1M}}