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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.020 1.000 2 2014 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.020 1.000 2 2013 2017
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.020 0.500 2 2012 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2016 2016
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2016 2016
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
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2010 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2017 2017
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2017 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
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
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2014 2014
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2019 2019
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
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.060 1.000 6 2010 2017
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
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