rs2416257, WDR36

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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.882 0.160 5 111099792 intron variant C/G;T snv 0.800 1.000 1 2009 2009
Asthma
CUI: C0004096
Disease: Asthma
1536 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2015 2015
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
23 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2010 2010
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2010 2010
Eosinophilic esophagitis
CUI: C0341106
Disease: Eosinophilic esophagitis
40 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2015 2015