Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121908585
rs121908585
0.827 0.080 4 54285926 missense variant A/T snv
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs121908587
rs121908587
0.827 0.120 4 54278380 missense variant C/T snv
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia
Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009