{{Rsnum
|rsid=6072161
|Chromosome=20
|position=40842787
|Orientation=plus
|GMAF=0.4444
|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 | 39.8 | 44.2 | 15.9
| HCB | 7.3 | 32.8 | 59.9
| JPT | 8.0 | 42.5 | 49.6
| YRI | 10.3 | 37.0 | 52.7
| ASW | 14.0 | 45.6 | 40.4
| CHB | 7.3 | 32.8 | 59.9
| CHD | 10.1 | 34.9 | 55.0
| GIH | 41.6 | 48.5 | 9.9
| LWK | 8.2 | 48.2 | 43.6
| MEX | 19.0 | 55.2 | 25.9
| MKK | 16.8 | 49.0 | 34.2
| TSI | 28.4 | 54.9 | 16.7
| 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-7
  |OR=.16
  |ORtxt=[0.098-0.22] 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}}