Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.500 GeneticVariation GWASDB A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274

2014
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.500 GeneticVariation GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605

2013
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.500 GeneticVariation GWASDB Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. 22700719

2012
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.500 GeneticVariation GWASDB We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461

2008
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation GWASDB Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. 23548203

2013
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0699893
Disease: Skin carcinoma
Skin carcinoma 		0.100 GeneticVariation GWASDB Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. 23548203

2013
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.100 GeneticVariation GWASDB Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort. 22704111

2012
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.100 GeneticVariation GWASDB Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235

2011
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		0.100 GeneticVariation GWASDB Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912

2011
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0015396
Disease: Eye Color
Eye Color 		0.100 GeneticVariation GWASDB Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627

2010
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0016689
Disease: Freckles
Freckles 		0.100 GeneticVariation GWASDB Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627

2010
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation GWASDB Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627

2010
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.100 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
Entrez Id: 3662
Gene Symbol: IRF4
IRF4
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation GWASDB A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. 18483556

2008