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.
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Left main coronary artery disease
CUI: C1299433
Disease: Left main coronary artery disease
4 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1 2018 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2018 2018
Osteomyelitis
CUI: C0029443
Disease: Osteomyelitis
14 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2018 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1 2019 2019
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2019 2019
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 0.010 1.000 1 2019 2019