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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.882 0.200 1 116561593 intron variant A/G snv 0.19 0.820 1.000 6 2009 2018
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.882 0.200 1 116561593 intron variant A/G snv 0.19 0.020 1.000 2 2014 2017
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.200 1 116561593 intron variant A/G snv 0.19 0.700 1.000 1 2017 2017