rs12550612, TNFRSF10C

N. diseases: 5
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.
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 8 23109256 intron variant G/A snv 0.83 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 8 23109256 intron variant G/A snv 0.83 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 8 23109256 intron variant G/A snv 0.83 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 8 23109256 intron variant G/A snv 0.83 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 8 23109256 intron variant G/A snv 0.83 0.700 1.000 1 2016 2016