{{Rsnum
|rsid=11847263
|Chromosome=14
|position=65308977
|Orientation=plus
|GMAF=0.4725
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 9.7 | 50.4 | 39.8
| HCB | 53.4 | 40.6 | 6.0
| JPT | 80.0 | 19.1 | 0.9
| YRI | 34.9 | 45.2 | 19.9
| ASW | 27.3 | 47.3 | 25.5
| CHB | 53.4 | 40.6 | 6.0
| CHD | 60.2 | 33.3 | 6.5
| GIH | 23.8 | 55.4 | 20.8
| LWK | 32.7 | 51.8 | 15.5
| MEX | 12.7 | 50.9 | 36.4
| MKK | 35.9 | 42.9 | 21.2
| TSI | 20.0 | 51.0 | 29.0
| 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=G
  |Pval=7E-14
  |OR=.24
  |ORtxt=[0.18-0.3] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}