{{Rsnum
|rsid=17103138
|Gene=TACC2
|Chromosome=10
|position=123913330
|Orientation=plus
|GMAF=0.1157
|Gene_s=TACC2
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 11.5 | 88.5
| HCB | 2.2 | 18.2 | 79.6
| JPT | 0.0 | 6.2 | 93.8
| YRI | 7.5 | 36.1 | 56.5
| ASW | 10.5 | 26.3 | 63.2
| CHB | 2.2 | 18.2 | 79.6
| CHD | 1.8 | 19.3 | 78.9
| GIH | 0.0 | 16.8 | 83.2
| LWK | 4.5 | 38.2 | 57.3
| MEX | 1.7 | 20.7 | 77.6
| MKK | 5.2 | 30.3 | 64.5
| TSI | 0.0 | 13.7 | 86.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=2E-7
  |OR=NR
  |ORtxt=NR
  }}

{{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}}