ACOXL, acyl-CoA oxidase like, 55289

N. diseases: 46; N. variants: 51
Disease: Microalbuminuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2880119
rs2880119
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0730345
Disease:
Microalbuminuria 		C 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532 2019