{{Rsnum
|rsid=2217262
|Gene=DOCK4
|Chromosome=7
|position=112156322
|Orientation=plus
|GMAF=0.08127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=DOCK4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 86.7 | 13.3 | 0.0
| HCB | 83.1 | 16.2 | 0.7
| JPT | 85.8 | 14.2 | 0.0
| YRI | 87.8 | 11.6 | 0.7
| ASW | 86.0 | 10.5 | 3.5
| CHB | 83.1 | 16.2 | 0.7
| CHD | 88.1 | 11.9 | 0.0
| GIH | 81.2 | 16.8 | 2.0
| LWK | 87.3 | 12.7 | 0.0
| MEX | 60.3 | 39.7 | 0.0
| MKK | 84.0 | 15.4 | 0.6
| TSI | 80.4 | 19.6 | 0.0
| HapMapRevision=28
}}[http://blog.23andme.com/2009/04/28/snpwatch-connections-between-brain-cells-may-be-key-to-autism-puzzle/ 23andMe blog] Wach copy of the A version of rs2217262 in the DOCK4 gene increased the odds of autism by 2.28 times.  Note that almost 90% of people with European ancestry have two copies of the A version of this SNP, meaning that these results really mean that the rare C version of the SNP is protective against [[autism]].

{{PMID Auto
|PMID=19401682
|Title=High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility
|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}}