rs1800566, NQO1

N. diseases: 59
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2013 2013
Alcohol withdrawal syndrome
CUI: C0236663
Disease: Alcohol withdrawal syndrome
6 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1 2003 2003
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2018 2018
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2015 2015
Cancer of Urinary Tract
CUI: C0751571
Disease: Cancer of Urinary Tract
11 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2015 2015
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2012 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2014 2014
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2008 2008
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 1999 1999
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2016 2016
Fast acetylator due to N-acetyltransferase enzyme variant
CUI: C1827820
Disease: Fast acetylator due to N-acetyltransferase enzyme variant
9 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2016 2016
Infant Acute Lymphoblastic Leukemia
CUI: C4054727
Disease: Infant Acute Lymphoblastic Leukemia
8 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2005 2005
leukemia
CUI: C0023418
Disease: leukemia
144 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2016 2016
Malignant mesothelioma
CUI: C0345967
Disease: Malignant mesothelioma
12 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2018 2018
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
55 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1 2014 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2011 2011
Malignant neoplasm of stomach stage IV
CUI: C0278498
Disease: Malignant neoplasm of stomach stage IV
7 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2014 2014
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2014 2014
melanoma
CUI: C0025202
Disease: melanoma
515 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2011 2011
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2008 2008
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1 2016 2016
nervous system disorder
CUI: C0027765
Disease: nervous system disorder
39 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2019 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2016 2016
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2011 2011