{{Rsnum
|rsid=11646213
|Chromosome=16
|position=82609046
|Orientation=plus
|GMAF=0.3669
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 15.4 | 49.2 | 35.4
| HCB | 72.1 | 23.3 | 4.7
| JPT | 63.6 | 31.8 | 4.5
| YRI | 62.3 | 36.1 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 72.1 | 23.3 | 4.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 54.7 | 37.7 | 7.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 44.1 | 44.7 | 11.2
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19304780
|Trait=Hypertension
|Title=Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations
|RiskAllele=T
|Pval=0.000008
|OR=1.28
|ORtxt=[1.15-1.43]
|OA=1
}}

{{PharmGKB
|RSID=rs11646213
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19304780; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. (Initial Sample Size: 364 cases, 590 controls; Replication Sample Size: 1,043 cases, 1,769 controls); (Region: 16q23.3; Reported Gene(s): CDH13; Risk Allele: rs11646213-T); (p-value= 0.000008).This variant is associated with Hypertension.
|Drugs=
|Drug Classes=
|Diseases=Hypertension
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739911
}}

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

{{PMID|21872196}} A variant upstream of the CDH13 adiponectin receptor gene and metabolic syndrome in Swedes.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11646213
|overall_frequency_n=44
|overall_frequency_d=128
|overall_frequency=0.34375
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=41
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=23976997
|Title=The Common Variant rs11646213 Is Associated with Preeclampsia in Han Chinese Women
|OA=1
}}

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