{{Rsnum
|rsid=1054611
|Gene=CLEC12B
|Chromosome=12
|position=10017562
|Orientation=plus
|GMAF=0.4555
|Gene_s=CLEC12B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 34.8 | 51.8 | 13.4
| HCB | 2.9 | 27.7 | 69.3
| JPT | 4.4 | 36.3 | 59.3
| YRI | 27.9 | 46.3 | 25.9
| ASW | 21.1 | 42.1 | 36.8
| CHB | 2.9 | 27.7 | 69.3
| CHD | 2.8 | 31.2 | 66.1
| GIH | 8.9 | 48.5 | 42.6
| LWK | 24.5 | 50.0 | 25.5
| MEX | 24.1 | 44.8 | 31.0
| MKK | 26.9 | 49.4 | 23.7
| TSI | 34.3 | 53.9 | 11.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23834954
  |Trait=Sensory disturbances after bilateral sagittal split ramus osteotomy
  |Title=Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.
  |RiskAllele=
  |Pval=6E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

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