{{Rsnum
|rsid=975334
|Gene=CNTN4
|Chromosome=3
|position=2804632
|Orientation=minus
|GMAF=0.4059
|Gene_s=CNTN4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 42.5 | 44.2 | 13.3
| HCB | 5.1 | 28.5 | 66.4
| JPT | 5.3 | 31.9 | 62.8
| YRI | 6.2 | 41.4 | 52.4
| ASW | 21.4 | 37.5 | 41.1
| CHB | 5.1 | 28.5 | 66.4
| CHD | 6.4 | 29.4 | 64.2
| GIH | 14.9 | 46.5 | 38.6
| LWK | 4.6 | 38.9 | 56.5
| MEX | 13.8 | 53.4 | 32.8
| MKK | 12.2 | 46.8 | 41.0
| TSI | 37.3 | 46.1 | 16.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22318345
|Trait=None
|Title=A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.
|RiskAllele=C
|Pval=9E-7
|OR=8.3000
|ORtxt=None
}}

{{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}}