rs12722489, IL2RA

N. diseases: 3
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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.882 0.160 10 6060049 intron variant C/T snv 0.11 0.850 1.000 7 2007 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.882 0.160 10 6060049 intron variant C/T snv 0.11 0.800 1.000 1 2010 2010
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.882 0.160 10 6060049 intron variant C/T snv 0.11 0.010 1 2011 2011