{{Rsnum
|rsid=2817461
|Chromosome=6
|position=156591878
|Orientation=minus
|GMAF=0.2328
|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 | 42.9 | 41.1 | 16.1
| HCB | 67.6 | 29.4 | 2.9
| JPT | 66.4 | 25.7 | 8.0
| YRI | 78.2 | 20.4 | 1.4
| ASW | 66.7 | 29.8 | 3.5
| CHB | 67.6 | 29.4 | 2.9
| CHD | 67.6 | 28.6 | 3.8
| GIH | 57.6 | 35.4 | 7.1
| LWK | 67.9 | 31.2 | 0.9
| MEX | 61.4 | 31.6 | 7.0
| MKK | 58.3 | 36.5 | 5.1
| TSI | 51.0 | 40.2 | 8.8
| 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=4E-8
  |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}}