rs385893, None

N. diseases: 9
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 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.800 1.000 2 2009 2019
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 5 2009 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2016 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2011 2011
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2016 2016
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
371 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2012 2012
Dengue Fever
CUI: C0011311
Disease: Dengue Fever
39 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.010 1.000 1 2016 2016