{{Rsnum
|rsid=2163237
|Chromosome=2
|position=55746597
|Orientation=minus
|GMAF=0.4017
|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 | 9.2 | 52.3 | 38.5
| HCB | 59.1 | 35.8 | 5.1
| JPT | 47.7 | 41.4 | 10.8
| YRI | 1.4 | 18.8 | 79.9
| ASW | 1.9 | 34.0 | 64.2
| CHB | 59.1 | 35.8 | 5.1
| CHD | 60.2 | 33.3 | 6.5
| GIH | 9.1 | 36.4 | 54.5
| LWK | 0.9 | 41.1 | 57.9
| MEX | 25.0 | 44.6 | 30.4
| MKK | 8.8 | 46.6 | 44.6
| TSI | 10.9 | 41.6 | 47.5
| 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=.15
  |ORtxt=[0.087-0.217] unit decrease
  |OA=1
}}

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