rs3917267, IL1R1

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.
Breakthrough infection
CUI: C3666010
Disease: Breakthrough infection
1 0.882 0.080 2 102162359 intron variant G/A snv 0.32 0.010 1.000 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.882 0.080 2 102162359 intron variant G/A snv 0.32 0.010 1.000 1 2017 2017
Infection in children
CUI: C3826128
Disease: Infection in children
5 0.882 0.080 2 102162359 intron variant G/A snv 0.32 0.010 1.000 1 2017 2017