{{Rsnum
|rsid=2140930
|Chromosome=11
|position=80600627
|Orientation=plus
|GMAF=0.3476
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LOC101928964
|Gene_s=LOC101928964
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.6 | 47.8 | 18.6
| HCB | 0.0 | 22.6 | 77.4
| JPT | 4.5 | 17.0 | 78.6
| YRI | 3.4 | 19.7 | 76.9
| ASW | 3.5 | 36.8 | 59.6
| CHB | 0.0 | 22.6 | 77.4
| CHD | 0.9 | 20.2 | 78.9
| GIH | 13.0 | 45.0 | 42.0
| LWK | 3.7 | 26.6 | 69.7
| MEX | 22.4 | 36.2 | 41.4
| MKK | 5.1 | 32.7 | 62.2
| TSI | 42.2 | 40.2 | 17.6
| 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=5E-6
  |OR=.17
  |ORtxt=[0.095-0.24] unit increase
  |OA=1
}}

{{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}}