{{Rsnum
|rsid=13236243
|Chromosome=7
|position=17278688
|Orientation=plus
|GMAF=0.3751
|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 | 48.7 | 41.6 | 9.7
| HCB | 35.8 | 49.6 | 14.6
| JPT | 37.5 | 49.1 | 13.4
| YRI | 29.3 | 55.8 | 15.0
| ASW | 35.1 | 54.4 | 10.5
| CHB | 35.8 | 49.6 | 14.6
| CHD | 39.4 | 45.0 | 15.6
| GIH | 37.6 | 45.5 | 16.8
| LWK | 30.9 | 47.3 | 21.8
| MEX | 32.8 | 34.5 | 32.8
| MKK | 30.1 | 48.7 | 21.2
| TSI | 58.8 | 32.4 | 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-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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}