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.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 9 111153625 intron variant T/C snv 0.21 0.700 1.000 3 2011 2017
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 9 111153625 intron variant T/C snv 0.21 0.700 1.000 3 2011 2017
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 9 111153625 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011