{{Rsnum
|rsid=7101378
|Chromosome=11
|position=109022640
|Orientation=plus
|GMAF=0.3388
|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 | 28.3 | 42.5 | 29.2
| HCB | 8.0 | 37.2 | 54.7
| JPT | 8.0 | 30.1 | 61.9
| YRI | 4.1 | 31.3 | 64.6
| ASW | 12.3 | 43.9 | 43.9
| CHB | 8.0 | 37.2 | 54.7
| CHD | 9.3 | 35.2 | 55.6
| GIH | 16.8 | 38.6 | 44.6
| LWK | 2.7 | 32.7 | 64.5
| MEX | 15.5 | 50.0 | 34.5
| MKK | 3.8 | 38.5 | 57.7
| TSI | 19.6 | 47.1 | 33.3
| 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=7E-6
  |OR=.14
  |ORtxt=[0.079-0.201] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}