rs1449263, None

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.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.700 1.000 3 2011 2018
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.700 1.000 3 2011 2018
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.700 1.000 1 2019 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.700 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.010 1.000 1 2007 2007