Source: GWASCAT

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 GWASCAT 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 GWASCAT 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 GWASCAT 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 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
PVT1
CUI: C0019829
Disease: Hodgkin 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: rs4410871
rs4410871
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs4410871
rs4410871
PVT1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT 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 		C 0.800 GeneticVariation GWASCAT A common variant at 8q24.21 is associated with renal cell cancer. 24220699

2013
dbSNP: rs11780156
rs11780156
PVT1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		T 0.710 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683

2017
dbSNP: rs11780156
rs11780156
PVT1
CUI: C0678222
Disease: Breast Carcinoma
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
PVT1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		T 0.710 GeneticVariation GWASCAT Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 23535729

2013
dbSNP: rs10087240
rs10087240
PVT1
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10087240
rs10087240
PVT1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10956401
rs10956401
PVT1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10956412
rs10956412
PVT1 ; MIR1208
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs11786130
rs11786130
PVT1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil 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: rs11786130
rs11786130
PVT1
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs12156002
rs12156002
PVT1
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017
dbSNP: rs12548864
rs12548864
PVT1
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs12548939
rs12548939
PVT1 ; TMEM75
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs12548939
rs12548939
PVT1 ; TMEM75
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs12676304
rs12676304
PVT1
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs13254990
rs13254990
PVT1
CUI: C2213246
Disease: Non-Hodgkin's lymphoma of central nervous system
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: rs13254990
rs13254990
PVT1
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. 25279986

2014
dbSNP: rs13255292
rs13255292
PVT1
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. 25261932

2014