rs2058660, IL18RAP

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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.882 0.280 2 102437989 intron variant G/A snv 0.78 0.810 1.000 2 2010 2015
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.882 0.280 2 102437989 intron variant G/A snv 0.78 0.010 1.000 1 2016 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.882 0.280 2 102437989 intron variant G/A snv 0.78 0.010 1.000 1 2012 2012
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.882 0.280 2 102437989 intron variant G/A snv 0.78 0.010 1.000 1 2015 2015