{{Rsnum
|rsid=3096277
|Gene=CDH13
|Chromosome=16
|position=83730599
|Orientation=plus
|GMAF=0.3136
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CDH13
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 55.4 | 40.0 | 4.6
| HCB | 15.9 | 56.1 | 28.0
| JPT | 23.2 | 38.4 | 38.4
| YRI | 38.7 | 46.5 | 14.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 15.9 | 56.1 | 28.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 46.5 | 43.4 | 10.1
| LWK | 58.1 | 36.2 | 5.7
| MEX | 72.7 | 23.6 | 3.6
| MKK | 0.0 | 0.0 | 0.0
| TSI | 74.2 | 23.7 | 2.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=17903302
|Trait=Blood pressure
|Title=Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
|RiskAllele=
|Pval=1.0000000000000001E-9
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto
|PMID=19304780
|Title=Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.
|OA=1
}}

{{PMID Auto
|PMID=19439027
|Title=Dissecting complex traits: recent advances in hypertension genomics.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3096277
|overall_frequency_n=85
|overall_frequency_d=128
|overall_frequency=0.664062
|n_genomes=44
|n_genomes_annotated=0
|n_haplomes=71
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}