Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.150 GeneticVariation GWASCAT Newly identified genetic risk variants for celiac disease related to the immune response. 18311140

2008
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.150 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.150 GeneticVariation GWASCAT Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235

2011
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.120 GeneticVariation GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199

2017
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.110 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		0.100 GeneticVariation GWASCAT Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. 25608926

2015
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0013595
Disease: Eczema
Eczema 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
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: 4026
Gene Symbol: LPP
LPP
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		0.100 GeneticVariation GWASCAT Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. 31477735

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.100 GeneticVariation GWASCAT A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. 29891935

2018
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.100 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		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: 4026
Gene Symbol: LPP
LPP
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.100 GeneticVariation GWASCAT Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. 29196614

2017
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.100 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017