{{Rsnum
|rsid=3757458
|Gene=CLDN15
|Chromosome=7
|position=101238122
|Orientation=plus
|GMAF=0.05051
|Gene_s=CLDN15
|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 | 0.0 | 7.1 | 92.9
| HCB | 1.5 | 17.5 | 81.0
| JPT | 0.9 | 21.2 | 77.9
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 7.0 | 93.0
| CHB | 1.5 | 17.5 | 81.0
| CHD | 0.9 | 17.4 | 81.7
| GIH | 1.0 | 14.9 | 84.2
| LWK | 0.0 | 0.9 | 99.1
| MEX | 1.7 | 8.6 | 89.7
| MKK | 0.0 | 0.6 | 99.4
| TSI | 0.0 | 6.9 | 93.1
| 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=2E-6
  |OR=8.00
  |ORtxt=[4.77-11.23] unit decrease
  |OA=1
}}

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