rs11465817, IL23R

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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.882 0.120 1 67255414 intron variant C/A;T snv 0.010 1.000 1 2009 2009
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.882 0.120 1 67255414 intron variant C/A;T snv 0.010 1.000 1 2013 2013
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.882 0.120 1 67255414 intron variant C/A;T snv 0.010 1.000 1 2013 2013
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.882 0.120 1 67255414 intron variant C/A;T snv 0.010 1.000 1 2013 2013