ACOXL, acyl-CoA oxidase like, 55289

N. diseases: 46; N. variants: 51
Disease: Microalbuminuria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532 2019