{{Rsnum
|rsid=1531590
|Chromosome=8
|position=75124209
|Orientation=plus
|GMAF=0.2925
|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 | 3.5 | 30.1 | 66.4
| HCB | 6.7 | 41.5 | 51.9
| JPT | 4.5 | 37.5 | 58.0
| YRI | 11.9 | 55.9 | 32.2
| ASW | 17.5 | 45.6 | 36.8
| CHB | 6.7 | 41.5 | 51.9
| CHD | 5.6 | 36.1 | 58.3
| GIH | 8.0 | 41.0 | 51.0
| LWK | 19.3 | 45.9 | 34.9
| MEX | 7.0 | 42.1 | 50.9
| MKK | 18.2 | 43.5 | 38.3
| TSI | 2.0 | 29.7 | 68.3
| 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=3E-6
  |OR=.18
  |ORtxt=[0.1-0.25] 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}}