rs1462059537, EDNRA

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 0.160 4 147535944 missense variant C/T snv 8.0E-06 0.030 1.000 3 2006 2015
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 0.020 1.000 2 2010 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 0.010 1.000 1 2012 2012
Renal sclerosis with hypertension
CUI: C0264657
Disease: Renal sclerosis with hypertension
9 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009