TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.953 190 2006 2020
dbSNP: rs12255372
rs12255372 		0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.908 65 2006 2020
dbSNP: rs7901695
rs7901695 		0.851 0.160 10 112994329 intron variant T/C snv 0.34
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 1.000 23 2006 2020
dbSNP: rs4506565
rs4506565 		0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.870 0.900 10 2006 2020
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.870 0.875 8 2008 2018
dbSNP: rs11196172
rs11196172 		0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.820 0.833 6 2014 2019
dbSNP: rs11196205
rs11196205 		0.827 0.200 10 113047288 intron variant G/A;C;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 0.917 12 2006 2020
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 9 2012 2019
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 5 2009 2019
dbSNP: rs4506565
rs4506565 		0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 4 2010 2019
dbSNP: rs4506565
rs4506565 		0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 2 2011 2016
dbSNP: rs11196174
rs11196174 		1.000 0.080 10 112974337 intron variant A/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.800 1.000 1 2013 2013
dbSNP: rs12243326
rs12243326 		0.925 0.160 10 113029056 intron variant T/C snv 0.27
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0.800 1.000 1 2010 2010
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0202098
Disease: Insulin measurement
Insulin measurement 		0.800 1.000 1 2011 2011
dbSNP: rs10885409
rs10885409 		1.000 0.080 10 113048313 intron variant T/C snv 0.54
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.720 1.000 4 2007 2015
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.720 1.000 3 2008 2011
dbSNP: rs7904519
rs7904519 		0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.710 1.000 4 2013 2018
dbSNP: rs12772424
rs12772424 		1.000 0.040 10 113120792 intron variant A/T snv 0.57
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.710 1.000 2 2014 2016
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.710 1.000 2 2019 2020
dbSNP: rs7903146
rs7903146 		0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.710 1.000 2 2011 2018
dbSNP: rs7904519
rs7904519 		0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.710 1.000 2 2013 2018
dbSNP: rs11196172
rs11196172 		0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172 		0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172 		0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172 		0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2014 2019