{{Rsnum
|rsid=6687262
|Chromosome=1
|position=79043424
|Orientation=plus
|GMAF=0.4536
|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 | 35.8 | 49.5 | 14.7
| HCB | 24.6 | 56.0 | 19.4
| JPT | 25.2 | 42.3 | 32.4
| YRI | 4.1 | 21.9 | 74.0
| ASW | 5.3 | 36.8 | 57.9
| CHB | 24.6 | 56.0 | 19.4
| CHD | 21.9 | 51.4 | 26.7
| GIH | 24.2 | 47.5 | 28.3
| LWK | 0.0 | 27.3 | 72.7
| MEX | 17.2 | 43.1 | 39.7
| MKK | 0.0 | 23.9 | 76.1
| TSI | 34.3 | 47.5 | 18.2
| 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=C
  |Pval=4E-7
  |OR=.16
  |ORtxt=[0.097-0.219] unit decrease
  |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}}