{{Rsnum
|rsid=7953959
|Chromosome=12
|position=97134362
|Orientation=plus
|GMAF=0.4931
|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 | 23.0 | 41.6 | 35.4
| HCB | 32.8 | 46.7 | 20.4
| JPT | 41.6 | 49.6 | 8.8
| YRI | 16.3 | 51.0 | 32.7
| ASW | 19.3 | 40.4 | 40.4
| CHB | 32.8 | 46.7 | 20.4
| CHD | 32.4 | 49.1 | 18.5
| GIH | 36.6 | 47.5 | 15.8
| LWK | 16.4 | 44.5 | 39.1
| MEX | 25.9 | 43.1 | 31.0
| MKK | 2.6 | 41.0 | 56.4
| TSI | 14.7 | 58.8 | 26.5
| 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=8E-6
  |OR=.14
  |ORtxt=[0.078-0.2] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}