{{Rsnum
|rsid=6064045
|Chromosome=20
|position=54084754
|Orientation=plus
|GMAF=0.3861
|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 | 26.5 | 45.1 | 28.3
| HCB | 55.1 | 41.2 | 3.7
| JPT | 32.7 | 51.8 | 15.5
| YRI | 68.7 | 28.6 | 2.7
| ASW | 68.4 | 28.1 | 3.5
| CHB | 55.1 | 41.2 | 3.7
| CHD | 59.3 | 34.3 | 6.5
| GIH | 47.0 | 44.0 | 9.0
| LWK | 71.6 | 26.6 | 1.8
| MEX | 17.5 | 47.4 | 35.1
| MKK | 64.1 | 32.7 | 3.2
| TSI | 13.9 | 43.6 | 42.6
| 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=.14
  |ORtxt=[0.077-0.197] 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}}