{{Rsnum
|rsid=793834
|Gene=DCDC2
|Chromosome=6
|position=24234705
|Orientation=minus
|GMAF=0.382
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DCDC2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 61.6 | 33.0 | 5.4
| HCB | 47.0 | 40.3 | 12.7
| JPT | 52.2 | 42.5 | 5.3
| YRI | 2.7 | 36.3 | 61.0
| ASW | 10.5 | 33.3 | 56.1
| CHB | 47.0 | 40.3 | 12.7
| CHD | 37.4 | 50.5 | 12.1
| GIH | 53.5 | 40.6 | 5.9
| LWK | 6.4 | 33.0 | 60.6
| MEX | 63.8 | 32.8 | 3.4
| MKK | 13.5 | 48.7 | 37.8
| TSI | 61.8 | 32.4 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21130836
|Trait=None
|Title=Whole genome association scan for genetic polymorphisms influencing information processing speed
|RiskAllele=A
|Pval=0.000003
|OR=0.1500
|ORtxt=[0.09-0.21] unit increase
|OA=1
}}

{{PMID Auto
|PMID=16385449
|Title=Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
|OA=1
}}

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