{{Rsnum
|rsid=4972806
|Chromosome=2
|position=176147850
|Orientation=plus
|GMAF=0.4793
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HOXD3
|Gene_s=HOXD3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 44.2 | 44.2 | 11.5
| HCB | 16.1 | 50.4 | 33.6
| JPT | 14.2 | 47.8 | 38.1
| YRI | 8.8 | 44.9 | 46.3
| ASW | 12.3 | 45.6 | 42.1
| CHB | 16.1 | 50.4 | 33.6
| CHD | 22.9 | 45.0 | 32.1
| GIH | 12.9 | 46.5 | 40.6
| LWK | 10.0 | 41.8 | 48.2
| MEX | 12.1 | 48.3 | 39.7
| MKK | 8.3 | 41.7 | 50.0
| TSI | 39.2 | 44.1 | 16.7
| 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=8E-6
  |OR=.14
  |ORtxt=[0.08-0.205] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}