{{Rsnum
|rsid=11619878
|Chromosome=13
|position=65637888
|Orientation=plus
|GMAF=0.3719
|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 | 30.1 | 52.2 | 17.7
| HCB | 0.0 | 15.3 | 84.7
| JPT | 0.9 | 17.7 | 81.4
| YRI | 14.3 | 56.5 | 29.3
| ASW | 21.1 | 50.9 | 28.1
| CHB | 0.0 | 15.3 | 84.7
| CHD | 4.6 | 13.8 | 81.7
| GIH | 23.8 | 51.5 | 24.8
| LWK | 20.9 | 44.5 | 34.5
| MEX | 22.4 | 55.2 | 22.4
| MKK | 16.0 | 56.4 | 27.6
| TSI | 18.6 | 47.1 | 34.3
| 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=1E-7
  |OR=.16
  |ORtxt=[0.1-0.22] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}