rs12266014, PRTFDC1

N. diseases: 7
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.
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 10 24922362 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016