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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
674 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.900 1.000 27 2007 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.900 0.952 24 2007 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
149 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.860 0.833 8 2009 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.850 0.800 6 2013 2016
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
160 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.800 1 2011 2011
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
1 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.700 4 2007 2009
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
745 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.700 1 2012 2012
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
29 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.700 1 2017 2017
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
108 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.700 1 2012 2012
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
192 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2016 2016
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
32 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2014 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2010 2012
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
141 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2013 2016
Diabetes Mellitus, Insulin-Dependent
775 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2009 2010
Hepatitis B Virus-Related Hepatocellular Carcinoma
5 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.020 1.000 2 2014 2016
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
17 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2007 2007
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
89 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2014 2014
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
17 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2007 2007
Arthritis
CUI: C0003864
Disease: Arthritis
25 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2013 2013
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
9 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2011 2011
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2011 2011
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
13 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2014 2014
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
696 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2010 2010
Crohn's disease of large bowel
CUI: C0156147
Disease: Crohn's disease of large bowel
1 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2011 2011
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
71 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1 2014 2014