{{Rsnum
|rsid=6102185
|Chromosome=20
|position=40849893
|Orientation=plus
|GMAF=0.3439
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 42.5 | 45.1 | 12.4
| HCB | 33.6 | 42.3 | 24.1
| JPT | 27.4 | 48.7 | 23.9
| YRI | 72.1 | 23.8 | 4.1
| ASW | 73.7 | 22.8 | 3.5
| CHB | 33.6 | 42.3 | 24.1
| CHD | 42.2 | 40.4 | 17.4
| GIH | 43.6 | 47.5 | 8.9
| LWK | 60.9 | 36.4 | 2.7
| MEX | 32.8 | 51.7 | 15.5
| MKK | 66.7 | 31.4 | 1.9
| TSI | 31.4 | 53.9 | 14.7
| 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=G
  |Pval=5E-6
  |OR=.14
  |ORtxt=[0.082-0.204] unit decrease
  |OA=1
}}

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