rs11572080, CYP2C8

N. diseases: 4
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 0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02 0.010 1.000 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02 0.010 1.000 1 2005 2005
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02 0.010 1.000 1 2013 2013