Source: GWASCAT ×
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
399 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.877 12 2005 2019
Diabetes Mellitus, Insulin-Dependent
198 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.950 6 2004 2020
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
439 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.972 6 2004 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
145 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.980 2 2005 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
57 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.857 1 2005 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
616 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.800 4 2005 2016
Vitiligo
CUI: C0042900
Disease: Vitiligo
87 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.900 2 2005 2018
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
17 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
185 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.800 1.000 2 2012 2019
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
17 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.800 1.000 1 2011 2012
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
98 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.760 0.857 1 2006 2019
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
29 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.740 1.000 1 2006 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
485 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.740 0.800 1 2008 2016
Diabetes Mellitus, Non-Insulin-Dependent
844 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.730 1.000 1 2008 2018
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
464 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.730 1.000 1 2011 2016
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
66 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.720 1.000 2 2006 2015
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
345 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.710 1.000 1 2016 2017
Latent Autoimmune Diabetes in Adults
6 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.710 1.000 1 2018 2019
Polymyositis
CUI: C0085655
Disease: Polymyositis
2 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.710 1.000 1 2008 2016
Myositis
CUI: C0027121
Disease: Myositis
39 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 2 2016 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1003 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 2 2016 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
130 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
130 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
130 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2019 2019
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2019 2019