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: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.830 GeneticVariation GWASCAT Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.830 GeneticVariation GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.830 GeneticVariation GWASDB Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. 22700719 2012
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.830 GeneticVariation GWASCAT Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. 22700719 2012
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.830 GeneticVariation BEFREE A recent genome wide association study of chronic lymphocytic leukaemia (CLL) provided evidence that common variation at 2q13 (rs17483466), 2q37.1 (rs13397985), 6p25.3 (rs872071), 11q24.1 (rs735665), 15q23 (rs7176508) and 19q13.32 (rs11083846) affects CLL risk. 20553269 2010
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.830 GeneticVariation BEFREE Common single nucleotide polymorphisms (SNPs) at 2q13 (rs17483466), 2q37.1 (rs13397985), 2q37.3 (rs757978), 6p25.3 (rs872071), 8q24.21 (rs2456449), 11q24.1 (rs735665), 15q21.3 (rs7169431), 15q23 (rs7176508), 16q24.1 (rs305061), and 19q13.32 (rs11083846) have been shown to confer a modest but significant increase in CLL risk. 20855867 2010
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.830 GeneticVariation GWASDB We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		0.830 GeneticVariation BEFREE We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
dbSNP: rs17483466
rs17483466
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.830 GeneticVariation GWASCAT We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
dbSNP: rs1439287
rs1439287
Entrez Id: 55289;400997;541471
Gene Symbol: ACOXL;ACOXL-AS1;MIR4435-2HG
ACOXL;ACOXL-AS1;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		A 0.800 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
dbSNP: rs1439287
rs1439287
Entrez Id: 55289;400997;541471
Gene Symbol: ACOXL;ACOXL-AS1;MIR4435-2HG
ACOXL;ACOXL-AS1;MIR4435-2HG
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		A 0.800 GeneticVariation GWASDB A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
dbSNP: rs6732565
rs6732565
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0003873
Disease:
Rheumatoid Arthritis 		A 0.800 GeneticVariation GWASCAT Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs6732565
rs6732565
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0003873
Disease:
Rheumatoid Arthritis 		A 0.800 GeneticVariation GWASDB Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs13401811
rs13401811
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
dbSNP: rs13401811
rs13401811
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
dbSNP: rs4849121
rs4849121
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0017661
Disease:
IGA Glomerulonephritis 		G 0.800 GeneticVariation GWASDB A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. 22197929 2011
dbSNP: rs4849121
rs4849121
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0017661
Disease:
IGA Glomerulonephritis 		G 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. 22197929 2011
dbSNP: rs11123201
rs11123201
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13413838
rs13413838
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs139153935
rs139153935
Entrez Id: 55289
Gene Symbol: ACOXL
ACOXL
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2009581
rs2009581
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2009581
rs2009581
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2009581
rs2009581
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
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
dbSNP: rs34931195
rs34931195
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019