CDH13, cadherin 13, 1012

N. diseases: 205; N. variants: 47
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4783244
rs4783244
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASDB A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2. 24105470 2014
dbSNP: rs4783244
rs4783244
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2. 24105470 2014
dbSNP: rs8057927
rs8057927
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0036341
Disease:
Schizophrenia
C 0.800 GeneticVariation GWASCAT Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. 23358160 2014
dbSNP: rs8057927
rs8057927
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0036341
Disease:
Schizophrenia
C 0.800 GeneticVariation GWASDB Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. 23358160 2014
dbSNP: rs9940464
rs9940464
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0024530
Disease:
Malaria
T 0.800 GeneticVariation GWASCAT Imputation-based meta-analysis of severe malaria in three African populations. 23717212 2013
dbSNP: rs9940464
rs9940464
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0024530
Disease:
Malaria
T 0.800 GeneticVariation GWASDB Imputation-based meta-analysis of severe malaria in three African populations. 23717212 2013
dbSNP: rs12051272
rs12051272
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
0.800 GeneticVariation GWASCAT We suggest that the phenotype-affecting haplotype tagged by rs12051272 SNP would affect the plasma adiponectin levels and that we have to take the CDH13 genotype into account before considering the functional relevance of the adiponectin level. 22065538 2012
dbSNP: rs12051272
rs12051272
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASCAT Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. 22479202 2012
dbSNP: rs12051272
rs12051272
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASDB Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. 22479202 2012
dbSNP: rs12051272
rs12051272
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
0.800 GeneticVariation GWASDB We suggest that the phenotype-affecting haplotype tagged by rs12051272 SNP would affect the plasma adiponectin levels and that we have to take the CDH13 genotype into account before considering the functional relevance of the adiponectin level. 22065538 2012
dbSNP: rs4783244
rs4783244
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
0.800 GeneticVariation GWASDB In addition, rs12051272 SNP genotypes in linkage disequilibrium with rs4783244 were found to be more significantly associated with adiponectin levels (P = 9.5×10(-20)) and specifically with the levels of high-molecular weight (HMW) adiponectin, a subtype form associated with parameters related to glucose metabolism. 22065538 2012
dbSNP: rs4783244
rs4783244
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASCAT We replicated and confirmed the association between rs4783244 and plasma adiponectin levels in an additional 559 YOH subjects (P = 5.70 × 10(-17)). 21771975 2011
dbSNP: rs4783244
rs4783244
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C2700366
Disease:
Adiponectin Measurement
T 0.800 GeneticVariation GWASDB We replicated and confirmed the association between rs4783244 and plasma adiponectin levels in an additional 559 YOH subjects (P = 5.70 × 10(-17)). 21771975 2011
dbSNP: rs140186760
rs140186760
Entrez Id: 1012;101928417
Gene Symbol: CDH13;LOC101928417
CDH13;LOC101928417
CUI: C0242350
Disease:
Erectile dysfunction
0.700 GeneticVariation GWASCAT GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology. 30583798 2019
dbSNP: rs2194285
rs2194285
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091 2019
dbSNP: rs2194285
rs2194285
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091 2019
dbSNP: rs7206608
rs7206608
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7206608
rs7206608
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0205682
Disease:
Waist-Hip Ratio
C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs7206608
rs7206608
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C1305855
Disease:
Body mass index
C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs7500448
rs7500448
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7500448
rs7500448
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0428883
Disease:
Diastolic blood pressure
G 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs11149581
rs11149581
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs11864066
rs11864066
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0596887
Disease:
mathematical ability
G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs4075464
rs4075464
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs4077666
rs4077666
Entrez Id: 1012
Gene Symbol: CDH13
CDH13
CUI: C0596887
Disease:
mathematical ability
C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018