{{Rsnum
|rsid=12367448
|Chromosome=12
|position=69187442
|Orientation=plus
|GMAF=0.1263
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 25.0 | 74.1
| HCB | 3.6 | 19.0 | 77.4
| JPT | 4.4 | 36.3 | 59.3
| YRI | 3.4 | 25.2 | 71.4
| ASW | 0.0 | 28.6 | 71.4
| CHB | 3.6 | 19.0 | 77.4
| CHD | 2.8 | 21.1 | 76.1
| GIH | 5.0 | 24.8 | 70.3
| LWK | 3.6 | 25.5 | 70.9
| MEX | 6.9 | 19.0 | 74.1
| MKK | 0.6 | 21.9 | 77.4
| TSI | 1.0 | 21.6 | 77.5
| 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=.25
  |ORtxt=[0.14-0.35] unit increase
  |OA=1
}}

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