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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 1.000 0.040 2 212959321 intron variant A/G snv 0.31 0.800 1.000 3 2009 2019
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
23 1.000 0.040 2 212959321 intron variant A/G snv 0.31 0.010 1.000 1 2010 2010
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 1.000 0.040 2 212959321 intron variant A/G snv 0.31 0.010 1.000 1 2010 2010