Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150684763
rs150684763
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17507216
rs17507216
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs17507216
rs17507216
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs783540
rs783540
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs3850610
rs3850610
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs783540
rs783540
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
dbSNP: rs783540
rs783540
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs1145170
rs1145170
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2303846
rs2303846
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0021364
Disease:
Male infertility 		0.010 GeneticVariation BEFREE Two SNPs from two genes (rs6631 of CGA and rs2303846 of CPEB1) were found to be associated with idiopathic male infertility. 21601192 2011
dbSNP: rs783540
rs783540
Entrez Id: 64506
Gene Symbol: CPEB1
CPEB1
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.010 GeneticVariation BEFREE A genome-wide association study of chronic lymphocytic leukaemia (CLL) suggested that common variants at 15q25.2 (rs783540) and 18q21.1 (rs1036935) influence CLL. 21554262 2011