Source: GWASDB ×
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
332 0.827 0.240 6 159069404 intron variant C/G;T snv 0.810 1.000 3 2010 2017
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
109 0.827 0.240 6 159069404 intron variant C/G;T snv 0.800 1.000 1 2011 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
104 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
104 0.827 0.240 6 159069404 intron variant C/G;T snv 0.700 1.000 1 2011 2011