{{Rsnum
|rsid=1339738
|Chromosome=1
|position=239233804
|Orientation=plus
|GMAF=0.07622
|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 | 0.9 | 18.6 | 80.5
| HCB | 2.9 | 26.3 | 70.8
| JPT | 1.8 | 21.2 | 77.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 1.8 | 98.2
| CHB | 2.9 | 26.3 | 70.8
| CHD | 0.9 | 19.3 | 79.8
| GIH | 1.0 | 12.9 | 86.1
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 5.2 | 94.8
| MKK | 0.0 | 10.9 | 89.1
| TSI | 1.0 | 19.6 | 79.4
| 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=7E-6
  |OR=.29
  |ORtxt=[0.16-0.42] unit increase
  |OA=1
}}

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