{{Rsnum
|rsid=7902627
|Chromosome=10
|position=33405087
|Orientation=plus
|GMAF=0.2052
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 73.5 | 24.8 | 1.8
| HCB | 63.5 | 32.1 | 4.4
| JPT | 52.2 | 44.2 | 3.5
| YRI | 36.7 | 48.3 | 15.0
| ASW | 45.6 | 36.8 | 17.5
| CHB | 63.5 | 32.1 | 4.4
| CHD | 60.6 | 36.7 | 2.8
| GIH | 80.2 | 18.8 | 1.0
| LWK | 28.2 | 51.8 | 20.0
| MEX | 81.0 | 19.0 | 0.0
| MKK | 27.6 | 57.7 | 14.7
| TSI | 80.4 | 19.6 | 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=8E-6
  |OR=.20
  |ORtxt=[0.11-0.29] unit decrease
  |OA=1
}}

{{on chip | Illumina Human 1M}}