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 0.827 0.240 6 159069404 intron variant C/G;T snv 0.810 1.000 6 2010 2017
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.827 0.240 6 159069404 intron variant C/G;T snv 0.800 1.000 2 2011 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.827 0.240 6 159069404 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.827 0.240 6 159069404 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.827 0.240 6 159069404 intron variant C/G;T snv 0.700 1.000 1 2015 2015
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.827 0.240 6 159069404 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.827 0.240 6 159069404 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.827 0.240 6 159069404 intron variant C/G;T snv 0.010 1.000 1 2014 2014