ACOXL, acyl-CoA oxidase like, 55289

N. diseases: 46; N. variants: 51
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3789087
rs3789087
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0200637
Disease:
Monocyte count procedure
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs150449635
rs150449635
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0200637
Disease:
Monocyte count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2062225
rs2062225
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0200637
Disease:
Monocyte count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3789088
rs3789088
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0200637
Disease:
Monocyte count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7578982
rs7578982
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0200637
Disease:
Monocyte count procedure
T 0.700 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011