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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.050 1.000 5 2010 2019
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.020 1.000 2 2013 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.010 1.000 1 2013 2013
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.010 1.000 1 2015 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.010 1.000 1 2019 2019
Pancolitis
CUI: C0868908
Disease: Pancolitis
11 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.360 1 67189464 intron variant G/A snv 0.29 0.010 1.000 1 2011 2011