{{Rsnum
|rsid=275456
|Chromosome=5
|position=6813824
|Orientation=minus
|GMAF=0.2199
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 6.2 | 41.1 | 52.7
| HCB | 4.4 | 36.5 | 59.1
| JPT | 8.8 | 39.8 | 51.3
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 10.5 | 89.5
| CHB | 4.4 | 36.5 | 59.1
| CHD | 3.7 | 29.4 | 67.0
| GIH | 12.9 | 43.6 | 43.6
| LWK | 0.0 | 5.5 | 94.5
| MEX | 8.8 | 49.1 | 42.1
| MKK | 0.6 | 14.7 | 84.6
| TSI | 7.8 | 41.2 | 51.0
| 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=3E-6
  |OR=2.26
  |ORtxt=[1.60-3.18]
  }}

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