rs17445836, None

N. diseases: 5
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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.851 0.320 16 85984057 intron variant G/A snv 0.15 0.700 1.000 1 2016 2016
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.851 0.320 16 85984057 intron variant G/A snv 0.15 0.010 1.000 1 2015 2015
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.851 0.320 16 85984057 intron variant G/A snv 0.15 0.010 1.000 1 2016 2016
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.851 0.320 16 85984057 intron variant G/A snv 0.15 0.010 1.000 1 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.851 0.320 16 85984057 intron variant G/A snv 0.15 0.810 1.000 2 2009 2011