{{Rsnum
|rsid=2965260
|Chromosome=19
|position=53276773
|Orientation=minus
|GMAF=0.1534
|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 | 0.9 | 18.6 | 80.5
| HCB | 3.6 | 40.1 | 56.2
| JPT | 6.2 | 27.4 | 66.4
| YRI | 4.1 | 36.1 | 59.9
| ASW | 3.5 | 35.1 | 61.4
| CHB | 3.6 | 40.1 | 56.2
| CHD | 3.7 | 24.8 | 71.6
| GIH | 3.0 | 24.8 | 72.3
| LWK | 0.9 | 30.0 | 69.1
| MEX | 1.7 | 24.1 | 74.1
| MKK | 1.3 | 21.2 | 77.6
| TSI | 0.0 | 21.6 | 78.4
| 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=9E-6
  |OR=.23
  |ORtxt=[0.13-0.33] 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}}