IFNG, interferon gamma, 3458

N. diseases: 1519; N. variants: 11
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: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.020 0.500 2 2012 2012
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.020 0.500 2 2012 2012
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.020 1.000 2 2010 2016
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0023281
Disease: Leishmaniasis
Leishmaniasis 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0024530
Disease: Malaria
Malaria 		Infections 0.010 1.000 1 2014 2014
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0002893
Disease: Refractory anemias
Refractory anemias 		Hemic and Lymphatic Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
Leishmaniasis, Cutaneous 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0085568
Disease: Buruli Ulcer
Buruli Ulcer 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0015967
Disease: Fever
Fever 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0026272
Disease: Mixed Connective Tissue Disease
Mixed Connective Tissue Disease 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705 		0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis 		Infections; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2069707
rs2069707 		0.925 0.120 12 68160508 intron variant G/A;C snv
CUI: C0031049
Disease: Pericarditis, Tuberculous
Pericarditis, Tuberculous 		Infections; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2069707
rs2069707 		0.925 0.120 12 68160508 intron variant G/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727 		0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2069727
rs2069727 		0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727 		0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs2069727
rs2069727 		0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2010 2010