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.
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
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 2 2012 2012
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
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
502 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2008 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2010 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2012 2016
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.554 0.680 10 112998590 intron variant C/G;T snv 0.710 1.000 2 2019 2020
Prediabetes syndrome
CUI: C0362046
Disease: Prediabetes syndrome
16 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2015 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2012 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2010 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.554 0.680 10 112998590 intron variant C/G;T snv 0.710 1.000 2 2011 2018
Adenocarcinoma of the gastroesophageal junction
6 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Atherogenic dyslipidaemia
CUI: C4524040
Disease: Atherogenic dyslipidaemia
9 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2009 2009
Autonomic neuropathy
CUI: C0259749
Disease: Autonomic neuropathy
7 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
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