rs3918181, NOS3

N. diseases: 2
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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.120 7 151004695 intron variant G/A snv 0.35 0.020 0.500 2 2013 2014
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.925 0.120 7 151004695 intron variant G/A snv 0.35 0.010 1.000 1 2014 2014