{{Rsnum
|rsid=2833991
|Chromosome=21
|position=32890379
|Orientation=plus
|GMAF=0.03857
|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 | 93.8 | 6.2 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 82.3 | 16.3 | 1.4
| ASW | 80.7 | 17.5 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 94.1 | 5.9 | 0.0
| LWK | 87.3 | 12.7 | 0.0
| MEX | 96.6 | 3.4 | 0.0
| MKK | 87.8 | 10.9 | 1.3
| TSI | 91.2 | 8.8 | 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=5E-6
  |OR=.35
  |ORtxt=[0.2-0.5] unit decrease
  |OA=1
}}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}