{{Rsnum
|rsid=10512385
|Chromosome=9
|position=108693295
|Orientation=plus
|GMAF=0.1208
|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 | 82.3 | 16.8 | 0.9
| HCB | 86.1 | 13.9 | 0.0
| JPT | 92.0 | 8.0 | 0.0
| YRI | 64.6 | 28.6 | 6.8
| ASW | 50.9 | 45.6 | 3.5
| CHB | 86.1 | 13.9 | 0.0
| CHD | 85.3 | 14.7 | 0.0
| GIH | 59.4 | 33.7 | 6.9
| LWK | 48.2 | 41.8 | 10.0
| MEX | 91.4 | 8.6 | 0.0
| MKK | 49.4 | 40.4 | 10.3
| TSI | 82.4 | 17.6 | 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=G
  |Pval=6E-6
  |OR=2.58
  |ORtxt=[1.71-3.89]
  }}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}