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.
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 1.000 6 2012 2018
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 1.000 6 2012 2018
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 9 2012 2019
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
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2008 2018
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
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
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
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
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
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
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
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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 0.900 10 2008 2019
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
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
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
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
CUI: C0011849
Disease: Diabetes Mellitus
824 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 1.000 37 2006 2020
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
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
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 1.000 35 2006 2020