{{Rsnum
|rsid=6435387
|Gene=KIF5C
|Chromosome=2
|position=149865250
|Orientation=plus
|GMAF=0.01791
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 10.6 | 89.4
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 2.1 | 97.9
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 3.0 | 97.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 3.5 | 96.5
| MKK | 0.0 | 0.6 | 99.4
| TSI | 0.0 | 7.9 | 92.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23453885
  |Trait=Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
  |Title=Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
  |RiskAllele=G
  |Pval=8E-6
  |OR=1.13
  |ORtxt=[1.06-1.19]
  |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}}