rs12255372, TCF7L2

N. diseases: 28
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.
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 0.667 3 2009 2018
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.667 0.480 10 113049143 intron variant G/A;T snv 0.070 0.857 7 2007 2019
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.667 0.480 10 113049143 intron variant G/A;T snv 0.900 0.908 65 2006 2020
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.667 0.480 10 113049143 intron variant G/A;T snv 0.090 1.000 9 2006 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.667 0.480 10 113049143 intron variant G/A;T snv 0.090 1.000 9 2006 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.667 0.480 10 113049143 intron variant G/A;T snv 0.050 1.000 5 2008 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.667 0.480 10 113049143 intron variant G/A;T snv 0.050 1.000 5 2008 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2016 2019
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2006 2011
Malignant neoplasm of colon and/or rectum
502 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2016 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2014 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.667 0.480 10 113049143 intron variant G/A;T snv 0.020 1.000 2 2009 2011
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2006 2006
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2011 2011
Diabetes in youth
CUI: C3825462
Disease: Diabetes in youth
2 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2011 2011
Diabetes Mellitus, Insulin-Dependent
954 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2010 2010
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.667 0.480 10 113049143 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.667 0.480 10 113049143 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2008 2008
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2008 2008
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
11 0.667 0.480 10 113049143 intron variant G/A;T snv 0.010 1.000 1 2009 2009