TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015396
Disease: Eye Color
Eye Color
0.100 GeneticVariation phenotype GWASDB Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010
CUI: C0015396
Disease: Eye Color
Eye Color
0.100 GeneticVariation phenotype GWASCAT Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010
CUI: C0015396
Disease: Eye Color
Eye Color
0.100 GeneticVariation phenotype GWASDB Genetic determinants of hair, eye and skin pigmentation in Europeans. 17952075 2007
CUI: C0015396
Disease: Eye Color
Eye Color
0.100 GeneticVariation phenotype GWASCAT Genetic determinants of hair, eye and skin pigmentation in Europeans. 17952075 2007