rs743506, NOS3

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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.925 0.120 7 151009827 intron variant G/A;C snv 0.020 1.000 2 2011 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.120 7 151009827 intron variant G/A;C snv 0.010 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.120 7 151009827 intron variant G/A;C snv 0.010 1.000 1 2015 2015
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.925 0.120 7 151009827 intron variant G/A;C snv 0.010 1.000 1 2015 2015