rs1258159645, NQO1

N. diseases: 37
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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2019 2019
nervous system disorder
CUI: C0027765
Disease: nervous system disorder
39 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2019 2019
Fast acetylator due to N-acetyltransferase enzyme variant
CUI: C1827820
Disease: Fast acetylator due to N-acetyltransferase enzyme variant
9 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2016 2016
Cancer of Urinary Tract
CUI: C0751571
Disease: Cancer of Urinary Tract
11 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2015 2015
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2014 2014
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2014 2014
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.020 1.000 2 2012 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1 2012 2012
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1 2012 2012
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2011 2017
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2011 2017
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2011 2017
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2011 2011
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.090 1.000 9 2010 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.090 1.000 9 2010 2019
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2008 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.040 0.750 4 2006 2014
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.040 0.750 4 2006 2014
Drug-induced tardive dyskinesia
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
67 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2006 2010
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
67 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2006 2010
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1 2006 2006
Infant Acute Lymphoblastic Leukemia
CUI: C4054727
Disease: Infant Acute Lymphoblastic Leukemia
8 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2005 2005