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 Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2007 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 190 2006 2020
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
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
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
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
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
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
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
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
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
Glioma
CUI: C0017638
Disease: Glioma
353 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
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
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
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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
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
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
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
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
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
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
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
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
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