{{Rsnum
|rsid=10090117
|Chromosome=8
|position=18523725
|Orientation=plus
|GMAF=0.1869
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.5 | 46.0 | 50.4
| HCB | 2.2 | 24.8 | 73.0
| JPT | 2.7 | 20.4 | 77.0
| YRI | 3.4 | 40.1 | 56.5
| ASW | 8.8 | 50.9 | 40.4
| CHB | 2.2 | 24.8 | 73.0
| CHD | 0.9 | 23.9 | 75.2
| GIH | 5.9 | 48.5 | 45.5
| LWK | 8.2 | 41.8 | 50.0
| MEX | 3.4 | 36.2 | 60.3
| MKK | 0.6 | 29.5 | 69.9
| TSI | 7.8 | 26.5 | 65.7
| 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=4E-6
  |OR=2.38
  |ORtxt=[1.64-3.44]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}