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.
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
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
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
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
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
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2019 2019
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
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
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
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2016 2016
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
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
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