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, Non-Insulin-Dependent
2672 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 190 2006 2020
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
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
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
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.554 0.680 10 112998590 intron variant C/G;T snv 0.710 1.000 2 2019 2020
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2020 2020
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
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
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
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
Latent autoimmune diabetes mellitus in adult
12 0.554 0.680 10 112998590 intron variant C/G;T snv 0.050 1.000 5 2008 2019
Diabetes Mellitus, Insulin-Dependent
954 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2007 2019
Latent Autoimmune Diabetes in Adults
12 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2019 2019
Adenocarcinoma of the gastroesophageal junction
6 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
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
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
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.554 0.680 10 112998590 intron variant C/G;T snv 0.870 0.875 8 2008 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
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
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
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
Malignant neoplasm of colon and/or rectum
502 0.554 0.680 10 112998590 intron variant C/G;T snv 0.020 1.000 2 2008 2018