ACOXL, acyl-CoA oxidase like, 55289

N. diseases: 46; N. variants: 51
Disease: Chronic Lymphocytic Leukemia ×
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