{{Rsnum
|rsid=918629
|Chromosome=5
|position=95965759
|Orientation=plus
|GMAF=0.4894
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CTD-2337A12.1
|Gene_s=CTD-2337A12.1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 37.2 | 55.8
| HCB | 70.1 | 28.5 | 1.5
| JPT | 62.8 | 31.9 | 5.3
| YRI | 39.0 | 45.9 | 15.1
| ASW | 45.6 | 40.4 | 14.0
| CHB | 70.1 | 28.5 | 1.5
| CHD | 76.1 | 22.9 | 0.9
| GIH | 20.8 | 49.5 | 29.7
| LWK | 43.6 | 41.8 | 14.5
| MEX | 13.8 | 51.7 | 34.5
| MKK | 42.9 | 47.4 | 9.6
| TSI | 5.9 | 32.4 | 61.8
| 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=1E-6
  |OR=.17
  |ORtxt=[0.1-0.24] unit increase
  |OA=1
}}

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