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.
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
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
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
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
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
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