{{Rsnum
|rsid=6494964
|Chromosome=15
|position=33201020
|Orientation=plus
|GMAF=0.4192
|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 | 39.8 | 53.1
| HCB | 27.7 | 54.7 | 17.5
| JPT | 38.9 | 42.5 | 18.6
| YRI | 37.0 | 48.6 | 14.4
| ASW | 22.8 | 56.1 | 21.1
| CHB | 27.7 | 54.7 | 17.5
| CHD | 34.9 | 38.5 | 26.6
| GIH | 5.0 | 33.7 | 61.4
| LWK | 29.1 | 48.2 | 22.7
| MEX | 17.2 | 44.8 | 37.9
| MKK | 27.6 | 55.1 | 17.3
| TSI | 5.9 | 40.2 | 53.9
| 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=6E-6
  |OR=.18
  |ORtxt=[0.1-0.26] unit increase
  |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}}