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.
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
20 0.878 0.071 9 5072846 intron variant G/A snp 0.24 0.010 1.000 1 2008 2008
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
22 0.878 0.071 9 5072846 intron variant G/A snp 0.24 0.010 1.000 1 2008 2008
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
18 0.878 0.071 9 5072846 intron variant G/A snp 0.24 0.010 1 2008 2008