{{Rsnum
|rsid=17179670
|Gene=HMGA2
|Chromosome=12
|position=65956032
|Orientation=plus
|GMAF=0.1309
|Gene_s=HMGA2
|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 | 70.5 | 25.0 | 4.5
| HCB | 87.6 | 12.4 | 0.0
| JPT | 87.6 | 12.4 | 0.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 87.6 | 12.4 | 0.0
| CHD | 89.9 | 10.1 | 0.0
| GIH | 46.0 | 41.0 | 13.0
| LWK | 96.3 | 3.7 | 0.0
| MEX | 63.8 | 31.0 | 5.2
| MKK | 89.1 | 9.6 | 1.3
| TSI | 53.9 | 40.2 | 5.9
| HapMapRevision=28
}}

Rs17179670 is a SNP implicated in [[Tooth Development]]

{{PMID Auto
|PMID=21358824
|Title=Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}