rs7288670, GGT5

N. diseases: 4
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 22 24225858 intron variant A/C;G snv 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 22 24225858 intron variant A/C;G snv 0.700 1.000 1 2016 2016
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 22 24225858 intron variant A/C;G snv 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 22 24225858 intron variant A/C;G snv 0.700 1.000 1 2016 2016