rs2069705, IFNG-AS1;IFNG

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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.695 0.440 12 68161231 intron variant G/A;C snv 0.020 0.500 2 2012 2012
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.695 0.440 12 68161231 intron variant G/A;C snv 0.020 1.000 2 2010 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.695 0.440 12 68161231 intron variant G/A;C snv 0.020 0.500 2 2012 2012
Asthma
CUI: C0004096
Disease: Asthma
1536 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2008 2008
Buruli Ulcer
CUI: C0085568
Disease: Buruli Ulcer
4 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2010 2010
Fever
CUI: C0015967
Disease: Fever
66 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2012 2012
Leishmaniasis
CUI: C0023281
Disease: Leishmaniasis
4 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Leishmaniasis, Cutaneous
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
17 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2016 2016
Malaria
CUI: C0024530
Disease: Malaria
148 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Mixed Connective Tissue Disease
CUI: C0026272
Disease: Mixed Connective Tissue Disease
4 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Pain
CUI: C0030193
Disease: Pain
196 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Refractory anemias
CUI: C0002893
Disease: Refractory anemias
11 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2020 2020
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2020 2020
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Superficial ulcer
CUI: C0333307
Disease: Superficial ulcer
10 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2020 2020
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2017 2017