rs4143832, None

N. diseases: 4
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.010 1 2013 2013
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.800 1.000 1 2009 2009
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
23 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.010 1.000 1 2010 2010
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.010 1.000 1 2010 2010