{{Rsnum
|rsid=3088362
|Gene=CCDC122
|Chromosome=13
|position=43859494
|Orientation=plus
|GMAF=0.2034
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CCDC122
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 35.4 | 64.6
| HCB | 8.1 | 44.4 | 47.4
| JPT | 8.0 | 35.7 | 56.2
| YRI | 2.0 | 23.1 | 74.8
| ASW | 3.5 | 19.3 | 77.2
| CHB | 8.1 | 44.4 | 47.4
| CHD | 2.8 | 34.3 | 63.0
| GIH | 11.9 | 36.6 | 51.5
| LWK | 2.8 | 25.2 | 72.0
| MEX | 6.9 | 43.1 | 50.0
| MKK | 2.6 | 26.3 | 71.2
| TSI | 5.0 | 25.7 | 69.3
| HapMapRevision=28
}}Variant in the [[CCDC122]] region associated with increased susceptibility to [[leprosy]] in Asians, according to the 23andMe blog [http://blog.23andme.com/2009/12/16/snpwatch-genetic-association-study-of-leprosy-yields-new-insights-into-an-ancient-disease/ 23andMe's blog]. The risk allele is A, and the odds ratio is 1.52.

{{omim
|id=613407
|rsnum=3088362
}}

{{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}}