rs10509681, CYP2C8

N. diseases: 8
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.
Acute gastrointestinal hemorrhage
CUI: C0266807
Disease: Acute gastrointestinal hemorrhage
4 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2007 2007
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2007 2007
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2005 2005
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2014 2014
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2013 2013