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.
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
206 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 0.700 1.000 14 2002 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 0.700 1.000 13 2002 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 0.700 0