Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		G 0.800 GeneticVariation GWASCAT A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. 26561523

2016
dbSNP: rs273909
rs273909
SLC22A4 ; MIR3936HG
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		A 0.800 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778

2018
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs10479002
rs10479002
SLC22A4 ; MIR3936HG
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		C 0.700 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
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		C 0.700 GeneticVariation GWASCAT A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. 30643255

2019
dbSNP: rs11950562
rs11950562
SLC22A4 ; MIR3936HG
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163

2019
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs270601
rs270601
SLC22A4 ; MIR3936HG
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415

2015
dbSNP: rs270602
rs270602
SLC22A4 ; MIR3936HG
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415

2015
dbSNP: rs272869
rs272869
SLC22A4 ; MIR3936HG
CUI: C0037369
Disease: Smoking
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625

2017
dbSNP: rs272869
rs272869
SLC22A4 ; MIR3936HG
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625

2017
dbSNP: rs34301845
rs34301845
SLC22A4 ; MIR3936HG
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs34301845
rs34301845
SLC22A4 ; MIR3936HG
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs419291
rs419291
SLC22A4
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163

2019
dbSNP: rs538021413
rs538021413
SLC22A4 ; MIR3936HG
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte 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: rs56399423
rs56399423
SLC22A4 ; MIR3936HG
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs6860806
rs6860806
SLC22A4
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		G 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683

2017