rs4851005, IL18R1

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.
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 2 102395092 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 2 102395092 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012