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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.080 15 34797231 intron variant G/A snv 0.45 0.010 1.000 1 2013 2013
Myopic macular degeneration
CUI: C0730271
Disease: Myopic macular degeneration
4 0.925 0.080 15 34797231 intron variant G/A snv 0.45 0.010 1.000 1 2015 2015