{{Rsnum
|rsid=1953652
|Chromosome=1
|position=86585518
|Orientation=plus
|GMAF=0.2837
|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 | 45.1 | 44.2 | 10.6
| HCB | 56.9 | 37.2 | 5.8
| JPT | 49.6 | 38.1 | 12.4
| YRI | 53.7 | 38.1 | 8.2
| ASW | 43.9 | 45.6 | 10.5
| CHB | 56.9 | 37.2 | 5.8
| CHD | 56.0 | 39.4 | 4.6
| GIH | 61.4 | 36.6 | 2.0
| LWK | 60.0 | 36.4 | 3.6
| MEX | 62.1 | 32.8 | 5.2
| MKK | 55.8 | 35.9 | 8.3
| TSI | 36.3 | 50.0 | 13.7
| 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=9E-6
  |OR=.14
  |ORtxt=[0.08-0.206] unit increase
  |OA=1
}}

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