rs4409785, None

N. diseases: 12
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.800 1.000 2 2014 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.800 1.000 1 2011 2011
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.800 1.000 1 2012 2012
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
76 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.752 0.240 11 95578258 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019