rs689470, PTGS2

N. diseases: 9
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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1 2006 2006
Esophagitis
CUI: C0014868
Disease: Esophagitis
7 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2010 2010
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2017 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1 2006 2006
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2012 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1 2006 2006
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2012 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2009 2009