SLC45A2, solute carrier family 45 member 2, 51151

N. diseases: 75; N. variants: 46
Disease: Eye Color ×
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 GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
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 Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010