{{Rsnum
|rsid=9394438
|Chromosome=6
|position=37564327
|Orientation=plus
|GMAF=0.4063
|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 | 14.2 | 46.0 | 39.8
| HCB | 39.7 | 48.5 | 11.8
| JPT | 44.2 | 44.2 | 11.5
| YRI | 0.0 | 26.5 | 73.5
| ASW | 5.3 | 36.8 | 57.9
| CHB | 39.7 | 48.5 | 11.8
| CHD | 52.3 | 39.4 | 8.3
| GIH | 17.8 | 37.6 | 44.6
| LWK | 3.6 | 28.2 | 68.2
| MEX | 15.5 | 41.4 | 43.1
| MKK | 1.3 | 31.4 | 67.3
| TSI | 10.8 | 43.1 | 46.1
| 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=.17
  |ORtxt=[0.094-0.24] 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}}