rs2293225, IL18RAP

N. diseases: 2
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.925 0.200 2 102419429 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.925 0.200 2 102419429 intron variant C/T snv 0.16 0.010 1.000 1 2017 2017