rs706779, IL2RA

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.
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.810 1.000 5 2010 2016
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
76 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.700 1.000 1 2012 2012
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.700 1.000 1 2012 2012
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.700 1.000 1 2012 2012
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.010 1.000 1 2015 2015