ACOXL, acyl-CoA oxidase like, 55289

N. diseases: 46; N. variants: 51
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17483466
rs17483466 		0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C2698259
Disease: Monoclonal B-Cell Lymphocytosis
Monoclonal B-Cell Lymphocytosis 		Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17483466
rs17483466 		0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs4849121
rs4849121 		0.925 0.160 2 110842129 intron variant G/A snv 0.44
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982 		2 111078961 intron variant T/C snv 0.27
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982 		2 111078961 intron variant T/C snv 0.27
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982 		2 111078961 intron variant T/C snv 0.27
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2011 2011
dbSNP: rs10207392
rs10207392 		2 111092082 intron variant A/G snv 0.48
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2012 2012
dbSNP: rs10207392
rs10207392 		2 111092082 intron variant A/G snv 0.48
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17483466
rs17483466 		0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		Male Urogenital Diseases; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs1866493
rs1866493 		2 111089501 intron variant A/T snv 0.41
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4849162
rs4849162 		2 110881658 intron variant T/C snv 0.32
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4849165
rs4849165 		2 110882012 intron variant T/C snv 0.33
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4849381
rs4849381 		2 111076804 intron variant G/C snv 0.26
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7575878
rs7575878 		2 111079087 intron variant A/C;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7578982
rs7578982 		2 111078961 intron variant T/C snv 0.27
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7599513
rs7599513 		2 111065699 intron variant A/C snv 0.31
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs875063
rs875063 		2 111055508 intron variant A/C snv 0.33
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17483466
rs17483466 		0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.830 1.000 5 2008 2013
dbSNP: rs17483466
rs17483466 		0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2008 2013
dbSNP: rs13401811
rs13401811 		0.925 0.120 2 110858527 intron variant G/A snv 0.19
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13401811
rs13401811 		0.925 0.120 2 110858527 intron variant G/A snv 0.19
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs1439287
rs1439287 		0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2014 2014
dbSNP: rs1439287
rs1439287 		0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs4849303
rs4849303 		0.790 0.080 2 110970905 intron variant C/G;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2014 2014
dbSNP: rs4849303
rs4849303 		0.790 0.080 2 110970905 intron variant C/G;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2014 2014