{{Rsnum
|rsid=12950390
|Chromosome=17
|position=47753582
|Orientation=plus
|GMAF=0.2066
|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 | 4.5 | 44.6 | 50.9
| HCB | 0.7 | 9.5 | 89.8
| JPT | 0.0 | 12.4 | 87.6
| YRI | 3.4 | 36.1 | 60.5
| ASW | 10.5 | 33.3 | 56.1
| CHB | 0.7 | 9.5 | 89.8
| CHD | 0.0 | 12.8 | 87.2
| GIH | 10.9 | 48.5 | 40.6
| LWK | 8.2 | 33.6 | 58.2
| MEX | 3.4 | 51.7 | 44.8
| MKK | 10.3 | 38.5 | 51.3
| TSI | 15.7 | 31.4 | 52.9
| 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=3E-6
  |OR=.17
  |ORtxt=[0.098-0.239] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}