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.
Human immunodeficiency virus (HIV) II infection category B1
56 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
183 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2015 2015
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
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
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
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
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
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
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
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
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
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
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
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
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
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
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