{{Rsnum
|rsid=6492998
|Gene=CHP
|Chromosome=15
|position=41254433
|Orientation=plus
|GMAF=0.3012
|Gene_s=CAMK4
|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 | 23.2 | 42.9 | 33.9
| HCB | 47.1 | 46.3 | 6.6
| JPT | 50.4 | 43.4 | 6.2
| YRI | 96.6 | 3.4 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 47.1 | 46.3 | 6.6
| CHD | 66.1 | 32.1 | 1.8
| GIH | 50.5 | 43.6 | 5.9
| LWK | 95.5 | 4.5 | 0.0
| MEX | 65.5 | 25.9 | 8.6
| MKK | 82.1 | 17.9 | 0.0
| TSI | 22.5 | 56.9 | 20.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21085126
|Title=SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population
}}

{{PMID Auto
|PMID=18628988
|Title=Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.
|OA=1
}}

{{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}}