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.
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.710 1.000 2 2013 2013
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.700 1.000 1 2011 2011
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.010 1.000 1 2014 2014
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.010 1.000 1 2019 2019