{{Rsnum
|rsid=12699683
|Chromosome=7
|position=15093502
|Orientation=plus
|GMAF=0.1194
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 85.8 | 14.2 | 0.0
| HCB | 69.1 | 24.3 | 6.6
| JPT | 65.5 | 31.0 | 3.5
| YRI | 88.7 | 11.3 | 0.0
| ASW | 78.9 | 19.3 | 1.8
| CHB | 69.1 | 24.3 | 6.6
| CHD | 61.1 | 35.2 | 3.7
| GIH | 89.9 | 10.1 | 0.0
| LWK | 82.6 | 17.4 | 0.0
| MEX | 66.7 | 31.6 | 1.8
| MKK | 73.2 | 24.8 | 2.0
| TSI | 85.3 | 14.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23776197
  |Trait=Paclitaxel-induced neuropathy
  |Title=Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy.
  |RiskAllele=A
  |Pval=7E-6
  |OR=3.66
  |ORtxt=[2.08-6.45]
  }}

{{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}}