Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2019960
rs2019960
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		C 0.800 GeneticVariation GWASDB A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. 24920014

2014
dbSNP: rs2019960
rs2019960
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		G 0.800 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013
dbSNP: rs2019960
rs2019960
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs2019960
rs2019960
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		G 0.800 GeneticVariation GWASDB 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
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		G 0.800 GeneticVariation GWASDB 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: rs4410871
rs4410871
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs6470588
rs6470588
PVT1
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.800 GeneticVariation GWASDB A common variant at 8q24.21 is associated with renal cell cancer. 24220699

2013
dbSNP: rs11780156
rs11780156
PVT1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		T 0.710 GeneticVariation GWASDB Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 23535729

2013
dbSNP: rs13255292
rs13255292
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		A 0.700 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013
dbSNP: rs4410871
rs4410871
PVT1
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		T 0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. 23817571

2013
dbSNP: rs4733809
rs4733809
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		A 0.700 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013
dbSNP: rs752427
rs752427
PVT1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		A 0.700 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013