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: C0042900
Disease: Vitiligo
Vitiligo 		0.100 GeneticVariation GWASCAT Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

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: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.100 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502

2012
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: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.100 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.100 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.100 GeneticVariation GWASCAT Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population. 22951725

2013
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.100 GeneticVariation GWASCAT A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. 25279986

2014
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: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414

2016
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: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.100 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.100 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma. 27424798

2016
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: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		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: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		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: C0243026
Disease: Sepsis
Sepsis 		0.100 GeneticVariation GWASCAT Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality. 27639821

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.100 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757

2016
Entrez Id: 4026
Gene Symbol: LPP
LPP
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