{{Rsnum
|rsid=17124610
|Chromosome=12
|position=61155300
|Orientation=plus
|GMAF=0.06566
|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 | 95.4 | 4.6 | 0.0
| HCB | 79.7 | 18.8 | 1.5
| JPT | 63.1 | 32.4 | 4.5
| YRI | 88.2 | 11.8 | 0.0
| ASW | 91.1 | 8.9 | 0.0
| CHB | 79.7 | 18.8 | 1.5
| CHD | 77.4 | 17.0 | 5.7
| GIH | 93.1 | 6.9 | 0.0
| LWK | 80.7 | 17.4 | 1.8
| MEX | 0.0 | 0.0 | 0.0
| MKK | 89.0 | 10.3 | 0.6
| TSI | 92.1 | 7.9 | 0.0
| 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=8E-6
  |OR=.67
  |ORtxt=[0.38-0.97] unit decrease
  |OA=1
}}

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