NQO1, NAD(P)H quinone dehydrogenase 1, 1728

N. diseases: 368; N. variants: 8
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: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2014 2020
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.100 1.000 11 2010 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.100 1.000 11 2010 2019
dbSNP: rs1258159645
rs1258159645
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.090 1.000 9 2010 2019
dbSNP: rs1258159645
rs1258159645
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.090 1.000 9 2010 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.070 0.714 7 2006 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.030 1.000 3 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.030 1.000 3 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.030 1.000 3 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.020 0.500 2 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.020 0.500 2 2012 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.020 0.500 2 2012 2019
dbSNP: rs1258159645
rs1258159645
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1258159645
rs1258159645
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.060 1.000 6 2011 2017
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.060 1.000 6 2011 2017
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.060 1.000 6 2011 2017
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2004 2017
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2004 2017
dbSNP: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2004 2017