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
745 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.810 1.000 2 2009 2011
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
419 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.700 1 2017 2017
Eosinophil count result
CUI: C0750879
Disease: Eosinophil count result
419 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.700 1 2017 2017
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
79 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.010 1.000 1 2016 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
225 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.010 1.000 1 2017 2017
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
44 0.846 0.286 16 85984057 intron variant G/A snp 0.17 0.010 1.000 1 2016 2016