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 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
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
metabolic disturbance
CUI: C0746556
Disease: metabolic disturbance
4 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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
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
Adenocarcinoma of the gastroesophageal junction
CUI: C1332166
Disease: 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
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
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
Glycosuria
CUI: C0017979
Disease: Glycosuria
7 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
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
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
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
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
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
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
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
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
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
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
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
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
Insulin measurement
CUI: C0202098
Disease: Insulin measurement
25 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 1 2011 2011
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
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2019 2019