{{Rsnum
|rsid=8079702
|Chromosome=17
|position=70194685
|Orientation=plus
|GMAF=0.478
|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 | 37.2 | 53.1 | 9.7
| HCB | 40.6 | 44.4 | 15.0
| JPT | 35.5 | 48.2 | 16.4
| YRI | 13.8 | 48.3 | 37.9
| ASW | 17.5 | 50.9 | 31.6
| CHB | 40.6 | 44.4 | 15.0
| CHD | 39.8 | 47.2 | 13.0
| GIH | 29.3 | 49.5 | 21.2
| LWK | 17.0 | 52.8 | 30.2
| MEX | 13.8 | 41.4 | 44.8
| MKK | 14.7 | 45.5 | 39.7
| TSI | 27.0 | 50.0 | 23.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20195514
|Trait=Primary tooth development (number of teeth)
|Title=Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy
|RiskAllele=G
|Pval=1E-14
|OR=1.15
|ORtxt=[NR] % variance explained
|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}}