{{Rsnum
|rsid=1039443
|Chromosome=5
|position=16037993
|Orientation=plus
|GMAF=0.1676
|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 | 3.5 | 28.3 | 68.1
| HCB | 0.0 | 21.2 | 78.8
| JPT | 0.9 | 15.9 | 83.2
| YRI | 21.1 | 51.7 | 27.2
| ASW | 7.0 | 50.9 | 42.1
| CHB | 0.0 | 21.2 | 78.8
| CHD | 0.0 | 22.9 | 77.1
| GIH | 1.0 | 26.7 | 72.3
| LWK | 12.7 | 50.9 | 36.4
| MEX | 0.0 | 13.8 | 86.2
| MKK | 16.7 | 42.9 | 40.4
| TSI | 2.9 | 20.6 | 76.5
| 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=8E-6
  |OR=.22
  |ORtxt=[0.12-0.32] 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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}