{{Rsnum
|rsid=4852708
|Gene=CD207
|Chromosome=2
|position=70836812
|Orientation=plus
|GMAF=0.1437
|Gene_s=CD207
|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 | 79.6 | 19.5 | 0.9
| HCB | 76.9 | 21.6 | 1.5
| JPT | 79.1 | 19.1 | 1.8
| YRI | 61.6 | 33.6 | 4.8
| ASW | 70.2 | 28.1 | 1.8
| CHB | 76.9 | 21.6 | 1.5
| CHD | 69.4 | 26.9 | 3.7
| GIH | 64.4 | 27.7 | 7.9
| LWK | 71.6 | 27.5 | 0.9
| MEX | 60.3 | 32.8 | 6.9
| MKK | 83.3 | 15.4 | 1.3
| TSI | 69.3 | 30.7 | 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=9E-6
  |OR=.21
  |ORtxt=[0.11-0.3] 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}}