SLC22A4, solute carrier family 22 member 4, 6583

N. diseases: 90; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1050152
rs1050152
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0010346
Disease:
Crohn Disease 		0.800 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
dbSNP: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0337428
Disease:
Fibrinogen assay 		C 0.800 GeneticVariation GWASDB 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: rs273909
rs273909
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1956346
Disease:
Coronary Artery Disease 		0.800 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125 2013
dbSNP: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1325327
Disease:
fibrinogen activity 		C 0.700 GeneticVariation GWASDB 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: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1561955
Disease:
Fibrinogen, CTCAE 		C 0.700 GeneticVariation GWASDB 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: rs270607
rs270607
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1561955
Disease:
Fibrinogen, CTCAE 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265 2011
dbSNP: rs270607
rs270607
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1325327
Disease:
fibrinogen activity 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265 2011
dbSNP: rs270607
rs270607
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0337428
Disease:
Fibrinogen assay 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265 2011
dbSNP: rs272888
rs272888
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
dbSNP: rs272889
rs272889
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0337438
Disease:
Glucose measurement 		A 0.700 GeneticVariation GWASDB Human metabolic individuality in biomedical and pharmaceutical research. 21886157 2011
dbSNP: rs272889
rs272889
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0495706
Disease:
elevated blood glucose level 		A 0.700 GeneticVariation GWASDB Human metabolic individuality in biomedical and pharmaceutical research. 21886157 2011
dbSNP: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0337428
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1956346
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0200638
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0857490
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0200633
Disease:
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: rs10075801
rs10075801
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0200641
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0023508
Disease:
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: rs10479002
rs10479002
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0337428
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0027430
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0200665
Disease:
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
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12777
rs12777
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0017654
Disease:
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: rs270601
rs270601
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0523446
Disease:
Acylcarnitines measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415 2015