rs5029939, TNFAIP3

N. diseases: 19
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
1172 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.850 1.000 6 2008 2017
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.800 1.000 1 2013 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.020 1.000 2 2010 2017
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2014 2014
Alveolitis, Fibrosing
CUI: C4721507
Disease: Alveolitis, Fibrosing
4 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2010 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2015 2015
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2014 2014
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
8 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2010 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2011 2011
Idiopathic pulmonary arterial hypertension
CUI: C3203102
Disease: Idiopathic pulmonary arterial hypertension
24 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2010 2010
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2010 2010
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2016 2016
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2011 2011
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2014 2014
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2015 2015
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2015 2015
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2015 2015
Polymyositis
CUI: C0085655
Disease: Polymyositis
22 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2014 2014
Pulmonary arterial hypertension
CUI: C2973725
Disease: Pulmonary arterial hypertension
70 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2010 2010