{{Rsnum
|rsid=2060070
|Chromosome=17
|position=56046612
|Orientation=plus
|GMAF=0.3682
|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 | 5.3 | 34.5 | 60.2
| HCB | 12.4 | 43.1 | 44.5
| JPT | 10.8 | 35.1 | 54.1
| YRI | 59.2 | 35.4 | 5.4
| ASW | 45.6 | 43.9 | 10.5
| CHB | 12.4 | 43.1 | 44.5
| CHD | 19.6 | 48.6 | 31.8
| GIH | 8.9 | 44.6 | 46.5
| LWK | 46.4 | 41.8 | 11.8
| MEX | 1.8 | 26.3 | 71.9
| MKK | 38.7 | 47.1 | 14.2
| TSI | 6.9 | 35.3 | 57.8
| 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=9E-7
  |OR=.18
  |ORtxt=[0.11-0.25] unit decrease
  |OA=1
}}

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