Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.400 GeneticVariation GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.400 GeneticVariation GWASCAT A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. 24920014

2014

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.400 GeneticVariation GWASCAT Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.400 GeneticVariation GWASCAT A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3). 21037568

2010

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.200 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.200 GeneticVariation GWASCAT Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. 25751625

2015

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.200 GeneticVariation GWASCAT Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 23535729

2013

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.140 GeneticVariation GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.140 GeneticVariation GWASCAT Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. 28346442

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.120 GeneticVariation GWASCAT A common variant at 8q24.21 is associated with renal cell cancer. 24220699

2013

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.100 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
Finding of Mean Corpuscular Hemoglobin
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
Non-Hodgkin's lymphoma of central nervous system
0.100 GeneticVariation GWASCAT A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC network study. 31102405

2019

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.100 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184

2018

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.100 GeneticVariation GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.100 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017

Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.100 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017