{{Rsnum
|rsid=10764775
|Chromosome=10
|position=130233808
|Orientation=plus
|GMAF=0.4853
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.5 | 44.2 | 44.2
| HCB | 50.0 | 40.4 | 9.6
| JPT | 36.0 | 45.0 | 18.9
| YRI | 39.5 | 49.0 | 11.6
| ASW | 26.3 | 50.9 | 22.8
| CHB | 50.0 | 40.4 | 9.6
| CHD | 54.1 | 42.2 | 3.7
| GIH | 22.8 | 46.5 | 30.7
| LWK | 40.0 | 40.9 | 19.1
| MEX | 12.1 | 58.6 | 29.3
| MKK | 21.8 | 46.8 | 31.4
| TSI | 10.8 | 44.1 | 45.1
| 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=C
  |Pval=6E-6
  |OR=.14
  |ORtxt=[0.081-0.206] 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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}