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.
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
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
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.554 0.680 10 112998590 intron variant C/G;T snv 0.090 0.444 9 2007 2017
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
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 0.667 3 2008 2010
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 0.667 3 2008 2010
Diabetes Mellitus, Insulin-Dependent
954 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2007 2019
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2006 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 0.833 6 2008 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.554 0.680 10 112998590 intron variant C/G;T snv 0.870 0.875 8 2008 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 0.900 10 2008 2019
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 0.944 18 2007 2019
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 190 2006 2020
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 1.000 37 2006 2020
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 1.000 35 2006 2020
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 9 2012 2019
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.554 0.680 10 112998590 intron variant C/G;T snv 0.070 1.000 7 2006 2020
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 1.000 6 2012 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 1.000 6 2012 2018
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 5 2009 2019
Latent autoimmune diabetes mellitus in adult
12 0.554 0.680 10 112998590 intron variant C/G;T snv 0.050 1.000 5 2008 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2011 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2008 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2008 2011