{{Rsnum
|rsid=7964407
|Chromosome=12
|position=28192989
|Orientation=minus
|GMAF=0.3209
|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 | 16.8 | 44.2 | 38.9
| HCB | 8.8 | 41.6 | 49.6
| JPT | 12.4 | 38.1 | 49.6
| YRI | 24.5 | 42.2 | 33.3
| ASW | 12.3 | 54.4 | 33.3
| CHB | 8.8 | 41.6 | 49.6
| CHD | 6.4 | 43.1 | 50.5
| GIH | 5.9 | 35.6 | 58.4
| LWK | 25.5 | 46.4 | 28.2
| MEX | 12.1 | 32.8 | 55.2
| MKK | 19.9 | 40.4 | 39.7
| TSI | 3.9 | 47.1 | 49.0
| 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=6E-6
  |OR=.21
  |ORtxt=[0.12-0.3] 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}}