rs10147992, STXBP6

N. diseases: 3
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 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011