Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4648310
rs4648310
PTGS2
1 186671393 downstream gene variant T/C;G snv
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2009 2009
dbSNP: rs4648308
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2010 2010
dbSNP: rs4648308
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 1.000 1 2010 2010
dbSNP: rs4648308
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.010 1.000 1 2017 2017
dbSNP: rs4648308
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2018 2018
dbSNP: rs4648308
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2010 2010
dbSNP: rs4648306
rs4648306
PTGS2
1.000 0.080 1 186671572 downstream gene variant C/T snv 0.12
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.010 1.000 1 2017 2017
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2009 2009
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 < 0.001 1 2006 2006
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 < 0.001 1 2006 2006
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2012 2012
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.010 1.000 1 2017 2017
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 < 0.001 1 2006 2006
dbSNP: rs689470
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0014868
Disease: Esophagitis
Esophagitis 		0.010 1.000 1 2010 2010
dbSNP: rs201931599
rs201931599
PTGS2
1.000 0.080 1 186671994 3 prime UTR variant T/A snv 1.7E-02
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.010 1.000 1 2017 2017
dbSNP: rs13306038
rs13306038
PTGS2
1.000 0.080 1 186671995 3 prime UTR variant A/T snv 4.6E-03
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.010 1.000 1 2017 2017
dbSNP: rs4648298
rs4648298
PTGS2
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2007 2007
dbSNP: rs4648298
rs4648298
PTGS2
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs4648298
rs4648298
PTGS2
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs13306035
rs13306035
PTGS2
1.000 0.080 1 186672715 3 prime UTR variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs2206593
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 < 0.001 1 2015 2015
dbSNP: rs2206593
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2015 2015
dbSNP: rs2206593
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 < 0.001 1 2015 2015