rs7903146, TCF7L2

N. diseases: 93
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.
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Nephritis, Interstitial
CUI: C0027707
Disease: Nephritis, Interstitial
5 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1 2014 2014
Nephritis, Tubulointerstitial
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
6 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1 2014 2014
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2020 2020
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
11 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Renal glomerular disease
CUI: C0268731
Disease: Renal glomerular disease
7 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2012 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Transient Cerebral Ischemia
CUI: C0917805
Disease: Transient Cerebral Ischemia
9 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Transient Ischemic Attack
CUI: C0007787
Disease: Transient Ischemic Attack
16 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2011 2011
TROPICAL CALCIFIC PANCREATITIS
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
13 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Type 2 diabetes mellitus in obese
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
4 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 0.500 2 2008 2014
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2008 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2008 2009
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2014 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2010 2015
Impaired insulin secretion
CUI: C0948379
Disease: Impaired insulin secretion
14 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2009 2010
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2011 2014
Latent Autoimmune Diabetes in Adults
CUI: C1739108
Disease: Latent Autoimmune Diabetes in Adults
12 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2019 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2008 2018