{{Rsnum
|rsid=27323
|Chromosome=5
|position=53256409
|Orientation=plus
|GMAF=0.455
|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 | 38.9 | 46.0 | 15.0
| HCB | 15.3 | 55.5 | 29.2
| JPT | 28.3 | 44.2 | 27.4
| YRI | 29.9 | 49.7 | 20.4
| ASW | 29.8 | 47.4 | 22.8
| CHB | 15.3 | 55.5 | 29.2
| CHD | 20.2 | 47.7 | 32.1
| GIH | 18.8 | 56.4 | 24.8
| LWK | 20.9 | 56.4 | 22.7
| MEX | 36.2 | 43.1 | 20.7
| MKK | 20.5 | 49.4 | 30.1
| TSI | 44.1 | 39.2 | 16.7
| 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=9E-6
  |OR=.14
  |ORtxt=[0.078-0.202] 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}}