{{Rsnum
|rsid=2900
|Chromosome=15
|position=23572574
|Orientation=minus
|GMAF=0.2328
|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 | 73.5 | 24.8 | 1.8
| HCB | 34.6 | 48.5 | 16.9
| JPT | 45.1 | 46.9 | 8.0
| YRI | 62.6 | 34.7 | 2.7
| ASW | 59.6 | 26.3 | 14.0
| CHB | 34.6 | 48.5 | 16.9
| CHD | 35.8 | 47.7 | 16.5
| GIH | 79.2 | 20.8 | 0.0
| LWK | 62.7 | 33.6 | 3.6
| MEX | 58.6 | 31.0 | 10.3
| MKK | 53.8 | 43.6 | 2.6
| TSI | 78.4 | 21.6 | 0.0
| 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=4E-6
  |OR=.20
  |ORtxt=[0.12-0.29] 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}}