{{Rsnum
|rsid=4789580
|Chromosome=17
|position=78315910
|Orientation=minus
|GMAF=0.3333
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 61.1 | 31.0 | 8.0
| HCB | 13.9 | 38.0 | 48.2
| JPT | 10.6 | 39.8 | 49.6
| YRI | 83.0 | 16.3 | 0.7
| ASW | 70.2 | 24.6 | 5.3
| CHB | 13.9 | 38.0 | 48.2
| CHD | 8.3 | 41.3 | 50.5
| GIH | 32.7 | 48.5 | 18.8
| LWK | 82.7 | 17.3 | 0.0
| MEX | 44.8 | 37.9 | 17.2
| MKK | 68.6 | 27.6 | 3.8
| TSI | 54.9 | 38.2 | 6.9
| 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=9E-6
  |OR=.23
  |ORtxt=[0.13-0.33] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}