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.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
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
Diabetes in youth
CUI: C3825462
Disease: Diabetes in youth
2 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2011 2011
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