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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.030 0.667 3 2006 2019
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2019 2019
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.050 0.800 5 2010 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.030 0.667 3 2011 2018
Osteomyelitis
CUI: C0029443
Disease: Osteomyelitis
14 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2018 2018
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
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
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
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1 2016 2016
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.040 0.500 4 2009 2015
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.040 0.500 4 2009 2015
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
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2012 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 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
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
Leukoencephalopathy
CUI: C0270612
Disease: Leukoencephalopathy
17 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1 2015 2015
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 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
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