Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10248298
rs10248298
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11764665
rs11764665
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1443749
rs1443749
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1899689
rs1899689
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C1305855
Disease:
Body mass index
T 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: rs1899692
rs1899692
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs983521
rs983521
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6466819
rs6466819
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
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: rs12706411
rs12706411
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0002395
Disease:
Alzheimer's Disease
T 0.700 GeneticVariation GWASCAT Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. 26830138 2016
dbSNP: rs17684427
rs17684427
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0474702
Disease:
Sulfate measurement
0.700 GeneticVariation GWASCAT From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases. 27412988 2016
dbSNP: rs80261602
rs80261602
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0037369
Disease:
Smoking
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs80261602
rs80261602
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs11767400
rs11767400
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C1314691
Disease:
Age at menarche
A 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs3757536
rs3757536
Entrez Id: 93664
Gene Symbol: CADPS2
CADPS2
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE In this cohort, we identified novel loci genome-wide significantly associated as modifiers of the age of onset of AD (CD44, rs187116, P=1.29 × 10⁻¹²; NPHP1, rs10173717, P=1.74 × 10⁻¹²; CADPS2, rs3757536, P=1.54 × 10⁻¹⁰; GREM2, rs12129547, P=1.69 × 10⁻¹³, among others) as well as other loci known to be associated with AD. 22710270 2013