{{Rsnum
|rsid=9984896
|Gene=CLDN14
|Chromosome=21
|position=36563371
|Orientation=plus
|GMAF=0.1175
|Gene_s=CLDN14
|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 | 51.3 | 42.5 | 6.2
| HCB | 86.9 | 13.1 | 0.0
| JPT | 80.5 | 16.8 | 2.7
| YRI | 99.3 | 0.7 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 86.9 | 13.1 | 0.0
| CHD | 90.8 | 7.3 | 1.8
| GIH | 69.3 | 29.7 | 1.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 92.9 | 7.1 | 0.0
| TSI | 73.5 | 23.5 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23166209
  |Trait=QT interval
  |Title=Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
  |RiskAllele=A
  |Pval=5E-6
  |OR=2.85
  |ORtxt=[1.63-4.07] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}