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
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
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
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
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
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
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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
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
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
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
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
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
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
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
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
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2012 2012
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
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