{{Rsnum
|rsid=2041670
|Gene=CLEC16A
|Chromosome=16
|position=11080795
|Orientation=plus
|GMAF=0.3388
|Gene_s=CLEC16A
|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 | 52.2 | 40.7 | 7.1
| HCB | 51.1 | 46.7 | 2.2
| JPT | 70.5 | 27.7 | 1.8
| YRI | 12.2 | 44.9 | 42.9
| ASW | 19.3 | 42.1 | 38.6
| CHB | 51.1 | 46.7 | 2.2
| CHD | 56.9 | 35.8 | 7.3
| GIH | 30.7 | 47.5 | 21.8
| LWK | 23.6 | 46.4 | 30.0
| MEX | 58.6 | 37.9 | 3.4
| MKK | 28.2 | 48.7 | 23.1
| TSI | 37.3 | 46.1 | 16.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=20849399
|Title=More CLEC16A gene variants associated with multiple sclerosis
}}

{{PMID Auto
|PMID=18840781
|Title=Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=20405052
|Title=The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
|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}}