{{Rsnum
|rsid=12213468
|Chromosome=6
|position=156336708
|Orientation=plus
|GMAF=0.1919
|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 | 7.1 | 33.6 | 59.3
| HCB | 2.2 | 16.1 | 81.8
| JPT | 1.8 | 9.7 | 88.5
| YRI | 0.0 | 13.6 | 86.4
| ASW | 0.0 | 22.8 | 77.2
| CHB | 2.2 | 16.1 | 81.8
| CHD | 0.9 | 18.3 | 80.7
| GIH | 5.9 | 41.6 | 52.5
| LWK | 1.8 | 12.7 | 85.5
| MEX | 13.8 | 29.3 | 56.9
| MKK | 1.3 | 22.4 | 76.3
| TSI | 9.8 | 46.1 | 44.1
| 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-6
  |OR=.15
  |ORtxt=[0.082-0.209] 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}}