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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: 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
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
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
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
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
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2007 2019
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
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
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
Latent autoimmune diabetes mellitus in adult
CUI: C1960272
Disease: 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
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
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.554 0.680 10 112998590 intron variant C/G;T snv 0.720 1.000 3 2008 2011
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2008 2013
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
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
Constitutional obesity
CUI: C2937224
Disease: Constitutional obesity
3 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Familial obesity
CUI: C1281440
Disease: Familial obesity
3 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008