{{Rsnum
|rsid=435066
|Chromosome=1
|position=68461830
|Orientation=plus
|GMAF=0.3163
|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 | 65.2 | 31.2 | 3.6
| HCB | 18.4 | 52.9 | 28.7
| JPT | 15.0 | 45.1 | 39.8
| YRI | 55.8 | 36.7 | 7.5
| ASW | 61.4 | 33.3 | 5.3
| CHB | 18.4 | 52.9 | 28.7
| CHD | 14.7 | 52.3 | 33.0
| GIH | 32.7 | 50.5 | 16.8
| LWK | 43.1 | 43.1 | 13.8
| MEX | 46.6 | 51.7 | 1.7
| MKK | 71.2 | 26.3 | 2.6
| TSI | 73.5 | 21.6 | 4.9
| 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=8E-6
  |OR=.18
  |ORtxt=[0.099-0.254] 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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}