{{Rsnum
|rsid=886126
|Gene=CUX2
|Chromosome=12
|position=111241410
|Orientation=plus
|GMAF=0.4463
|Gene_s=CUX2
|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 | 55.8 | 43.4 | 0.9
| HCB | 13.1 | 39.4 | 47.4
| JPT | 11.5 | 48.7 | 39.8
| YRI | 13.6 | 44.2 | 42.2
| ASW | 7.0 | 63.2 | 29.8
| CHB | 13.1 | 39.4 | 47.4
| CHD | 11.0 | 45.9 | 43.1
| GIH | 35.0 | 51.0 | 14.0
| LWK | 17.3 | 50.0 | 32.7
| MEX | 41.4 | 51.7 | 6.9
| MKK | 23.1 | 51.3 | 25.6
| TSI | 56.9 | 32.4 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23364394
  |Trait=Coronary heart disease
  |Title=A genome-wide association study of a coronary artery disease risk variant.
  |RiskAllele=T
  |Pval=1E-6
  |OR=1.14
  |ORtxt=[1.08-1.20]
  }}

{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}