{{Rsnum
|rsid=2063640
|Chromosome=3
|position=102484201
|Orientation=plus
|GMAF=0.1621
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 14.2 | 85.0
| HCB | 6.6 | 41.6 | 51.8
| JPT | 14.2 | 48.7 | 37.2
| YRI | 0.0 | 8.8 | 91.2
| ASW | 1.8 | 7.0 | 91.2
| CHB | 6.6 | 41.6 | 51.8
| CHD | 9.2 | 34.9 | 56.0
| GIH | 1.0 | 20.8 | 78.2
| LWK | 0.0 | 1.8 | 98.2
| MEX | 5.2 | 39.7 | 55.2
| MKK | 0.0 | 1.3 | 98.7
| TSI | 0.0 | 21.6 | 78.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21490949
|Trait=None
|Title=Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
|RiskAllele=A
|Pval=0.000003
|OR=1.2300
|ORtxt=[1.13-1.34]
|OA=1
}}

{{PMID Auto
|PMID=23834954
|Title=Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy
|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}}