rs2430561, IFNG;IFNG-AS1

N. diseases: 50
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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2012 2012
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2017 2017
Asthma
CUI: C0004096
Disease: Asthma
1536 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1 2014 2014
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2012 2012
Boutonneuse Fever
CUI: C0006060
Disease: Boutonneuse Fever
3 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2009 2009
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.020 1.000 2 2014 2014
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2015 2015
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2015 2015
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
20 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1 2013 2013
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2014 2014
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2010 2010
Generalized vitiligo
CUI: C1304470
Disease: Generalized vitiligo
16 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2013 2013
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2014 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2017 2017
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1 2019 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2016 2016
Kidney Failure, Acute
CUI: C0022660
Disease: Kidney Failure, Acute
32 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2014 2014