{{Rsnum
|rsid=17666538
|Chromosome=8
|position=616207
|Orientation=plus
|GMAF=0.0528
|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 | 0.9 | 12.4 | 86.7
| HCB | 0.0 | 16.1 | 83.9
| JPT | 0.9 | 8.8 | 90.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 16.1 | 83.9
| CHD | 0.0 | 12.0 | 88.0
| GIH | 1.0 | 4.0 | 95.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 4.9 | 95.1
| 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=7E-6
  |OR=.28
  |ORtxt=[0.16-0.41] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}