{{Rsnum
|rsid=11079764
|Chromosome=17
|position=47232327
|Orientation=plus
|GMAF=0.3802
|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 | 19.5 | 56.6 | 23.9
| HCB | 43.1 | 47.4 | 9.5
| JPT | 54.9 | 36.3 | 8.8
| YRI | 74.8 | 20.4 | 4.8
| ASW | 43.9 | 49.1 | 7.0
| CHB | 43.1 | 47.4 | 9.5
| CHD | 36.7 | 50.5 | 12.8
| GIH | 12.9 | 46.5 | 40.6
| LWK | 76.4 | 20.0 | 3.6
| MEX | 43.1 | 50.0 | 6.9
| MKK | 39.6 | 47.4 | 13.0
| TSI | 14.7 | 45.1 | 40.2
| 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=5E-6
  |OR=.18
  |ORtxt=[0.1-0.26] 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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}