Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.200 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.100 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163

2019
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		0.100 GeneticVariation GWASCAT A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. 30643255

2019
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778

2018
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0037369
Disease: Smoking
Smoking 		0.100 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625

2017
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.100 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683

2017
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.100 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625

2017
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
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
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.100 GeneticVariation GWASCAT A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. 26561523

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415

2015
Entrez Id: 6583
Gene Symbol: SLC22A4
SLC22A4
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.100 GeneticVariation GWASCAT Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577

2009