IRF4, interferon regulatory factor 4, 3662

N. diseases: 203; N. variants: 10
Disease: Hair Color ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. 23548203 2013
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASDB Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. 23548203 2013
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASCAT Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASDB Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASDB A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. 18483556 2008
CUI: C0018498
Disease: Hair Color
Hair Color 		0.100 GeneticVariation phenotype GWASCAT A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. 18483556 2008