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.
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: 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
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
Hereditary Multiple Exostoses
CUI: C0015306
Disease: Hereditary Multiple Exostoses
51 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: 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
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2006 2017
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.554 0.680 10 112998590 intron variant C/G;T snv 0.070 1.000 7 2006 2020
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
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
Hip circumference
CUI: C0562350
Disease: Hip circumference
116 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2015 2015
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
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
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
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
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 5 2009 2019
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
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 0.944 18 2007 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2014 2018
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
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
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