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: 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
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.100 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406

2017
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: 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: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. 25429064

2015
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: 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 Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 23535729

2013
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: 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: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. 25261932

2014
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
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
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
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
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 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: 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: 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: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.100 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017