{{Rsnum
|rsid=8048207
|Gene=CDH8
|Chromosome=16
|position=61744191
|Orientation=plus
|GMAF=0.1506
|Gene_s=CDH8
|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 | 86.5 | 13.5 | 0.0
| HCB | 85.9 | 11.9 | 2.2
| JPT | 72.3 | 22.3 | 5.4
| YRI | 36.1 | 52.4 | 11.6
| ASW | 50.0 | 32.1 | 17.9
| CHB | 85.9 | 11.9 | 2.2
| CHD | 86.1 | 13.9 | 0.0
| GIH | 86.1 | 12.9 | 1.0
| LWK | 44.5 | 48.2 | 7.3
| MEX | 77.2 | 21.1 | 1.8
| MKK | 41.0 | 50.6 | 8.3
| TSI | 85.1 | 14.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23144319
  |Trait=Non-small cell lung cancer
  |Title=Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.
  |RiskAllele=T
  |Pval=8E-6
  |OR=NR
  |ORtxt=NR
  }}

{{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}}