Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
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
ACOXL ; MIR4435-2HG
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
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
ACOXL ; MIR4435-2HG
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
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: rs13401811
rs13401811
ACOXL
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605

2013
dbSNP: rs1439287
rs1439287
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		A 0.800 GeneticVariation GWASDB A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274

2014
dbSNP: rs4849121
rs4849121
ACOXL
CUI: C0017661
Disease: IGA Glomerulonephritis
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: rs6732565
rs6732565
ACOXL
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		A 0.800 GeneticVariation GWASDB Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342

2014
dbSNP: rs10207392
rs10207392
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		G 0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.700 GeneticVariation GWASDB Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort. 22704111

2012
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs1866493
rs1866493
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs4849162
rs4849162
ACOXL
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs4849165
rs4849165
ACOXL
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs4849381
rs4849381
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs7575878
rs7575878
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		T 0.700 GeneticVariation GWASDB Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478

2011
dbSNP: rs7599513
rs7599513
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs875063
rs875063
ACOXL ; MIR4435-2HG
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012