rs689466, PACERR;PTGS2

N. diseases: 33
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.
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.020 1.000 2 2011 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.020 1.000 2 2010 2011
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2010 2010
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2010 2010
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1 2010 2010
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2010 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1 2010 2010