Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 2 2011 2016
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs3731211
rs3731211
9 21986848 intron variant T/A snv 0.74
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016