{{Rsnum
|rsid=6833812
|Gene=STK32B
|Chromosome=4
|position=5108413
|Orientation=plus
|GMAF=0.1846
|Gene_s=STK32B
|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 | 8.0 | 29.2 | 62.8
| HCB | 1.5 | 22.1 | 76.5
| JPT | 2.7 | 23.0 | 74.3
| YRI | 4.8 | 31.3 | 63.9
| ASW | 5.3 | 33.3 | 61.4
| CHB | 1.5 | 22.1 | 76.5
| CHD | 1.8 | 32.1 | 66.1
| GIH | 5.0 | 41.6 | 53.5
| LWK | 2.8 | 18.5 | 78.7
| MEX | 3.4 | 31.0 | 65.5
| MKK | 1.9 | 25.0 | 73.1
| TSI | 10.8 | 23.5 | 65.7
| 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=7E-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 | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}