{{Rsnum
|rsid=7248637
|Gene=CD209
|Chromosome=19
|position=7742141
|Orientation=plus
|GMAF=0.214
|Gene_s=CD209
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 18.6 | 77.9
| HCB | 15.3 | 39.4 | 45.3
| JPT | 6.2 | 35.7 | 58.0
| YRI | 15.6 | 40.1 | 44.2
| ASW | 19.3 | 45.6 | 35.1
| CHB | 15.3 | 39.4 | 45.3
| CHD | 11.0 | 38.5 | 50.5
| GIH | 4.0 | 24.8 | 71.3
| LWK | 11.8 | 39.1 | 49.1
| MEX | 0.0 | 25.9 | 74.1
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 16.7 | 83.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=23576520
|Title=Genetic Polymorphisms in Host Innate Immune Sensor Genes and the Risk of Nasopharyngeal Carcinoma in North Africa
|OA=1
}}

{{PMID Auto
|PMID=23650115
|Title=Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}