{{Rsnum
|rsid=2708240
|Gene=CNTNAP2
|Chromosome=7
|position=147880445
|Orientation=plus
|GMAF=0.3999
|Gene_s=CNTNAP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 29.2 | 46.9 | 23.9
| HCB | 32.8 | 45.3 | 21.9
| JPT | 51.3 | 44.2 | 4.4
| YRI | 48.3 | 42.9 | 8.8
| ASW | 42.1 | 47.4 | 10.5
| CHB | 32.8 | 45.3 | 21.9
| CHD | 30.3 | 48.6 | 21.1
| GIH | 17.8 | 55.4 | 26.7
| LWK | 51.4 | 37.6 | 11.0
| MEX | 39.7 | 43.1 | 17.2
| MKK | 60.9 | 34.0 | 5.1
| TSI | 29.4 | 48.0 | 22.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23459443
  |Trait=QT interval (interaction)
  |Title=Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
  |RiskAllele=A
  |Pval=4E-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 | Illumina Human 1M}}