{{Rsnum
|rsid=10877839
|Chromosome=12
|position=62424701
|Orientation=plus
|GMAF=0.3021
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.7 | 38.7 | 49.5
| HCB | 15.4 | 50.0 | 34.6
| JPT | 21.4 | 45.5 | 33.0
| YRI | 0.0 | 8.8 | 91.2
| ASW | 0.0 | 26.3 | 73.7
| CHB | 15.4 | 50.0 | 34.6
| CHD | 16.5 | 54.1 | 29.4
| GIH | 4.0 | 24.8 | 71.3
| LWK | 0.0 | 8.3 | 91.7
| MEX | 6.9 | 39.7 | 53.4
| MKK | 0.0 | 1.9 | 98.1
| TSI | 7.8 | 43.1 | 49.0
| 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=9E-6
  |OR=.15
  |ORtxt=[0.082-0.21] 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}}