rs1801058, GRK4

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 0.040 1.000 4 2010 2017
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 0.030 1.000 3 2006 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 0.010 1.000 1 2015 2015