{{Rsnum
|rsid=12455580
|Chromosome=18
|position=77926067
|Orientation=plus
|GMAF=0.4885
|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 | 44.5 | 40.9 | 14.5
| HCB | 39.4 | 48.2 | 12.4
| JPT | 31.9 | 58.4 | 9.7
| YRI | 2.7 | 29.3 | 68.0
| ASW | 3.5 | 28.1 | 68.4
| CHB | 39.4 | 48.2 | 12.4
| CHD | 43.0 | 43.9 | 13.1
| GIH | 30.7 | 45.5 | 23.8
| LWK | 10.0 | 36.4 | 53.6
| MEX | 37.9 | 55.2 | 6.9
| MKK | 24.4 | 46.8 | 28.8
| TSI | 27.5 | 44.1 | 28.4
| 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=7E-6
  |OR=.16
  |ORtxt=[0.091-0.23] unit increase
  |OA=1
}}

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