{{Rsnum
|rsid=998592
|Gene=CLEC16A
|Chromosome=16
|position=11105821
|Orientation=minus
|GMAF=0.348
|Gene_s=CLEC16A
|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 | 10.6 | 46.0 | 43.4
| HCB | 4.4 | 50.4 | 45.3
| JPT | 8.8 | 39.8 | 51.3
| YRI | 8.2 | 42.2 | 49.7
| ASW | 14.0 | 43.9 | 42.1
| CHB | 4.4 | 50.4 | 45.3
| CHD | 11.9 | 49.5 | 38.5
| GIH | 24.2 | 46.5 | 29.3
| LWK | 12.7 | 36.4 | 50.9
| MEX | 10.3 | 41.4 | 48.3
| MKK | 9.6 | 59.6 | 30.8
| TSI | 25.5 | 46.1 | 28.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=20849399
|Title=More CLEC16A gene variants associated with multiple sclerosis
}}

{{PMID Auto
|PMID=22534877
|Title=Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}