PLPP3, phospholipid phosphatase 3, 8613

N. diseases: 8; N. variants: 13
Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17114036
rs17114036
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0010068
Disease:
Coronary heart disease
0.800 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014
dbSNP: rs17114036
rs17114036
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0010068
Disease:
Coronary heart disease
A 0.800 GeneticVariation GWASCAT Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990 2011
dbSNP: rs17114046
rs17114046
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0010068
Disease:
Coronary heart disease
0.800 GeneticVariation GWASCAT A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease. 21846871 2011
dbSNP: rs17114046
rs17114046
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0010068
Disease:
Coronary heart disease
0.800 GeneticVariation GWASCAT A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. 21378988 2011
dbSNP: rs55869368
rs55869368
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs61772626
rs61772626
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs75264190
rs75264190
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs147055617
rs147055617
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs17114046
rs17114046
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
G 0.700 GeneticVariation GWASCAT Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. 30104761 2018
dbSNP: rs17114046
rs17114046
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs17416285
rs17416285
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
C 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs4634932
rs4634932
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs2404715
rs2404715
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0871470
Disease:
Systolic Pressure
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs56170783
rs56170783
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
A 0.700 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975 2017
dbSNP: rs72664324
rs72664324
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0206161
Disease:
Reticulocyte count (procedure)
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9970807
rs9970807
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C1956346
Disease:
Coronary Artery Disease
C 0.700 GeneticVariation GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387 2015
dbSNP: rs9970807
rs9970807
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0027051
Disease:
Myocardial Infarction
C 0.700 GeneticVariation GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387 2015
dbSNP: rs11206830
rs11206830
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0341106
Disease:
Eosinophilic esophagitis
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104 2014
dbSNP: rs17114036
rs17114036
Entrez Id: 8613
Gene Symbol: PLPP3
PLPP3
CUI: C0038454
Disease:
Cerebrovascular accident
0.700 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014