rs5051, AGT

N. diseases: 5
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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.882 0.160 1 230714126 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.160 1 230714126 intron variant C/A;G;T snv 0.020 1.000 2 2013 2014
Erythrocytosis due to low atmospheric pressure
CUI: C0272139
Disease: Erythrocytosis due to low atmospheric pressure
13 0.882 0.160 1 230714126 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 1 230714126 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.160 1 230714126 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013