rs899115126, EDNRA

N. diseases: 3
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.
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.080 4 147542603 missense variant G/C snv 0.010 1.000 1 2006 2006
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.882 0.080 4 147542603 missense variant G/C snv 0.010 1.000 1 2006 2006
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
56 0.882 0.080 4 147542603 missense variant G/C snv 0.010 1.000 1 2016 2016