PVT1, Pvt1 oncogene, 5820

N. diseases: 27; N. variants: 31
Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2019960
rs2019960
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease:
Hodgkin Disease 		C 0.800 GeneticVariation GWASCAT A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. 24920014 2014
dbSNP: rs2019960
rs2019960
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease:
Hodgkin Disease 		G 0.800 GeneticVariation GWASCAT Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102 2013
dbSNP: rs4410871
rs4410871
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602 2013
dbSNP: rs6470588
rs6470588
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0007134
Disease:
Renal Cell Carcinoma 		C 0.800 GeneticVariation GWASCAT A common variant at 8q24.21 is associated with renal cell cancer. 24220699 2013
dbSNP: rs2019960
rs2019960
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs4410871
rs4410871
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs2019960
rs2019960
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease:
Hodgkin Disease 		G 0.800 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
dbSNP: rs2608053
rs2608053
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0019829
Disease:
Hodgkin Disease 		G 0.800 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
dbSNP: rs11780156
rs11780156
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.710 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs11780156
rs11780156
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.710 GeneticVariation GWASCAT Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. 25751625 2015
dbSNP: rs11780156
rs11780156
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.710 GeneticVariation GWASCAT Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 23535729 2013
dbSNP: rs10956401
rs10956401
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10956412
rs10956412
Entrez Id: 5820;100302281
Gene Symbol: PVT1;MIR1208
PVT1;MIR1208
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12676304
rs12676304
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13254990
rs13254990
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C2213246
Disease:
Non-Hodgkin's lymphoma of central nervous system 		T 0.700 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
dbSNP: rs1499364
rs1499364
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2608029
rs2608029
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005612
Disease:
Birth Weight 		G 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs4733823
rs4733823
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs66824612
rs66824612
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6992123
rs6992123
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6992491
rs6992491
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs6470578
rs6470578
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C2607914
Disease:
Allergic rhinitis (disorder) 		T 0.700 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184 2018
dbSNP: rs12156002
rs12156002
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469 2017
dbSNP: rs13280095
rs13280095
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.700 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469 2017
dbSNP: rs2608029
rs2608029
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		G 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730 2017