{{Rsnum
|rsid=7845056
|Chromosome=8
|position=141939370
|Orientation=plus
|GMAF=0.4353
|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 | 21.2 | 42.5 | 36.3
| HCB | 44.5 | 41.6 | 13.9
| JPT | 47.8 | 39.8 | 12.4
| YRI | 85.7 | 14.3 | 0.0
| ASW | 57.9 | 31.6 | 10.5
| CHB | 44.5 | 41.6 | 13.9
| CHD | 31.2 | 47.7 | 21.1
| GIH | 17.8 | 39.6 | 42.6
| LWK | 85.3 | 14.7 | 0.0
| MEX | 17.2 | 43.1 | 39.7
| MKK | 73.7 | 25.0 | 1.3
| TSI | 20.6 | 42.2 | 37.3
| 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=9E-6
  |OR=.18
  |ORtxt=[0.099-0.256] unit increase
  |OA=1
}}

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