Source: GWASDB ×
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
1613 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.877 8 2005 2019
Diabetes Mellitus, Insulin-Dependent
477 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.950 4 2004 2020
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
104 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.980 1 2005 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
93 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.857 1 2005 2019
Vitiligo
CUI: C0042900
Disease: Vitiligo
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.900 3 2005 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
332 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.800 2 2005 2016
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
1 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.850 0.667 1 2006 2017
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
42 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.800 1.000 1 2012 2019
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
104 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.800 1.000 1 2011 2012
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
56 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.740 1.000 1 2008 2015
Asthma
CUI: C0004096
Disease: Asthma
263 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2011 2011
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
49 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
488 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2011 2011