{{Rsnum
|rsid=4141404
|Gene=LIMK2
|Chromosome=22
|position=31279199
|Orientation=minus
|GMAF=0.1763
|Gene_s=LIMK2
|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 | 50.4 | 38.1 | 11.5
| HCB | 73.7 | 25.5 | 0.7
| JPT | 75.2 | 24.8 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 89.5 | 10.5 | 0.0
| CHB | 73.7 | 25.5 | 0.7
| CHD | 71.6 | 28.4 | 0.0
| GIH | 51.5 | 46.5 | 2.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 53.4 | 34.5 | 12.1
| MKK | 97.4 | 2.6 | 0.0
| TSI | 58.8 | 36.3 | 4.9
| 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=2.41
  |ORtxt=[1.66-3.48]
  }}

{{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}}