{{Rsnum
|rsid=1604897
|Chromosome=8
|position=121170070
|Orientation=plus
|GMAF=0.3338
|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 | 69.0 | 29.2 | 1.8
| HCB | 36.8 | 41.9 | 21.3
| JPT | 26.8 | 50.9 | 22.3
| YRI | 21.8 | 45.6 | 32.7
| ASW | 38.6 | 47.4 | 14.0
| CHB | 36.8 | 41.9 | 21.3
| CHD | 29.4 | 45.9 | 24.8
| GIH | 36.6 | 46.5 | 16.8
| LWK | 23.6 | 55.5 | 20.9
| MEX | 69.0 | 24.1 | 6.9
| MKK | 36.5 | 46.8 | 16.7
| TSI | 66.7 | 25.5 | 7.8
| 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=.19
  |ORtxt=[0.1-0.27] 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}}