TNFAIP3, TNF alpha induced protein 3, 7128

N. diseases: 212; N. variants: 29
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5029924
rs5029924 		0.851 0.200 6 137866361 intron variant C/T snv 0.13
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs5029924
rs5029924 		0.851 0.200 6 137866361 intron variant C/T snv 0.13
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs5029924
rs5029924 		0.851 0.200 6 137866361 intron variant C/T snv 0.13
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs5029924
rs5029924 		0.851 0.200 6 137866361 intron variant C/T snv 0.13
CUI: C0242966
Disease: Systemic Inflammatory Response Syndrome
Systemic Inflammatory Response Syndrome 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs583522
rs583522 		0.925 0.080 6 137868747 intron variant C/A;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs583522
rs583522 		0.925 0.080 6 137868747 intron variant C/A;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs583522
rs583522 		0.925 0.080 6 137868747 intron variant C/A;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs5029928
rs5029928 		1.000 6 137868805 intron variant C/T snv 0.20
CUI: C0544015
Disease: Fuchs' syndrome
Fuchs' syndrome 		0.010 < 0.001 1 2014 2014
dbSNP: rs3757173
rs3757173 		1.000 0.080 6 137869017 intron variant A/G snv 0.20
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.720 1.000 3 2012 2016
dbSNP: rs5029930
rs5029930 		1.000 0.040 6 137869547 intron variant A/C snv 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs719149
rs719149 		1.000 0.120 6 137871608 intron variant G/A snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs719150
rs719150 		6 137871624 intron variant A/G snv 0.20
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5029937
rs5029937 		0.882 0.160 6 137874014 intron variant G/T snv 0.13
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.740 1.000 5 2009 2017
dbSNP: rs5029937
rs5029937 		0.882 0.160 6 137874014 intron variant G/T snv 0.13
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.710 1.000 2 2009 2016
dbSNP: rs5029937
rs5029937 		0.882 0.160 6 137874014 intron variant G/T snv 0.13
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs5029937
rs5029937 		0.882 0.160 6 137874014 intron variant G/T snv 0.13
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs598493
rs598493 		1.000 0.120 6 137874265 intron variant T/C snv 0.71
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs643177
rs643177 		1.000 0.040 6 137874556 intron variant T/C snv 0.70
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 2 2015 2015
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.850 1.000 6 2008 2017
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.020 1.000 2 2010 2017
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension 		Respiratory Tract Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs5029939
rs5029939 		0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2014 2014