{{Rsnum
|rsid=2270954
|Gene=DCC
|Chromosome=18
|position=53530928
|Orientation=plus
|GMAF=0.1671
|Gene_s=DCC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 22.1 | 77.9
| HCB | 2.9 | 38.7 | 58.4
| JPT | 5.3 | 36.3 | 58.4
| YRI | 2.7 | 32.0 | 65.3
| ASW | 5.3 | 31.6 | 63.2
| CHB | 2.9 | 38.7 | 58.4
| CHD | 3.7 | 40.4 | 56.0
| GIH | 3.0 | 25.7 | 71.3
| LWK | 2.7 | 30.0 | 67.3
| MEX | 0.0 | 27.6 | 72.4
| MKK | 2.6 | 18.6 | 78.8
| TSI | 2.9 | 26.5 | 70.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=22418395
|Title=Association between schizophrenia and genetic variation in DCC: A case-control study
}}

The PMID above is interesting. It found an association between [[rs2270954]] and schizophrenia. Patients were most likely to be homozygous for the minor allele. The study suggests that the DCC gene may contribute to individual genetic differences in susceptibility to schizophrenia. This SNP is located within the 3' untranslated region, an area known to contain a number of regulatory sequences that determine the stability and translation efficacy of mRNA.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}