{{Rsnum
|rsid=4869266
|Chromosome=5
|position=96151236
|Orientation=plus
|GMAF=0.3783
|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 | 15.9 | 42.5 | 41.6
| HCB | 26.7 | 37.8 | 35.6
| JPT | 36.4 | 50.0 | 13.6
| YRI | 9.7 | 35.2 | 55.2
| ASW | 7.0 | 38.6 | 54.4
| CHB | 26.7 | 37.8 | 35.6
| CHD | 15.7 | 59.3 | 25.0
| GIH | 7.9 | 47.5 | 44.6
| LWK | 3.7 | 32.7 | 63.6
| MEX | 35.1 | 45.6 | 19.3
| MKK | 6.5 | 41.9 | 51.6
| TSI | 16.7 | 42.2 | 41.2
| 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=3E-6
  |OR=.15
  |ORtxt=[0.088-0.216] unit increase
  |OA=1
}}

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