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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.554 0.680 10 112998590 intron variant C/G;T snv 0.710 1.000 2 2011 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
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
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
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.554 0.680 10 112998590 intron variant C/G;T snv 0.090 0.444 9 2007 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 0.833 6 2008 2017
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
Prediabetes syndrome
CUI: C0362046
Disease: Prediabetes syndrome
16 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2015 2017
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
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
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
Physical Activity Measurement
CUI: C4049938
Disease: Physical Activity Measurement
355 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Smoking
CUI: C0037369
Disease: Smoking
765 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2012 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2012 2016
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2016 2016
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
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
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
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