rs3842787, PTGS1

N. diseases: 11
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.
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.030 0.667 3 2006 2015
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1 2004 2004
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2007 2007
Bleeding ulcer
CUI: C0333291
Disease: Bleeding ulcer
1 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2006 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1 2011 2011
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2013 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 0.010 1.000 1 2015 2015