{{Rsnum
|rsid=2094962
|Chromosome=9
|position=134924613
|Orientation=minus
|GMAF=0.2433
|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 | 0.9 | 12.4 | 86.7
| HCB | 0.7 | 26.3 | 73.0
| JPT | 0.0 | 25.0 | 75.0
| YRI | 55.1 | 35.4 | 9.5
| ASW | 28.1 | 50.9 | 21.1
| CHB | 0.7 | 26.3 | 73.0
| CHD | 1.8 | 33.9 | 64.2
| GIH | 1.0 | 17.8 | 81.2
| LWK | 49.1 | 47.3 | 3.6
| MEX | 1.7 | 27.6 | 70.7
| MKK | 31.4 | 53.2 | 15.4
| TSI | 1.0 | 22.5 | 76.5
| 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=5E-6
  |OR=.24
  |ORtxt=[0.14-0.34] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}