{{Rsnum
|rsid=10198756
|Chromosome=2
|position=219999933
|Orientation=plus
|GMAF=0.3356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 68.8 | 25.9 | 5.4
| HCB | 13.9 | 48.9 | 37.2
| JPT | 10.6 | 46.0 | 43.4
| YRI | 31.3 | 57.8 | 10.9
| ASW | 43.9 | 50.9 | 5.3
| CHB | 13.9 | 48.9 | 37.2
| CHD | 15.6 | 57.8 | 26.6
| GIH | 46.5 | 46.5 | 6.9
| LWK | 45.0 | 47.7 | 7.3
| MEX | 46.6 | 41.4 | 12.1
| MKK | 46.8 | 44.2 | 9.0
| TSI | 75.5 | 24.5 | 0.0
| 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=3E-6
  |OR=.21
  |ORtxt=[0.12-0.29] 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 | Illumina Human 1M}}