rs20417, PACERR;PTGS2

N. diseases: 57
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.
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2015 2016
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.050 0.800 5 2010 2018
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2012 2015
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
28 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.030 0.667 3 2006 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.030 1.000 3 2011 2015
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2010 2010
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2010 2010
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2009 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2009 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.030 1.000 3 2009 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2009 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2010 2010
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2003 2003
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2016 2016
Esophagitis
CUI: C0014868
Disease: Esophagitis
7 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2010 2010
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2017 2017