{{Rsnum
|rsid=9467076
|Gene=DCDC2
|Chromosome=6
|position=24209027
|Orientation=plus
|GMAF=0.09229
|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 | 0.0 | 20.0 | 80.0
| HCB | 2.2 | 4.4 | 93.3
| JPT | 0.0 | 4.5 | 95.5
| YRI | 0.0 | 23.8 | 76.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 4.4 | 93.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20068590
|Title=[[Dyslexia]] and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
|OA=1
}}
{{omim
|id=600202
|rsnum=9467076
}}{{PMID|16385449|OA=1
}} Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.