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: 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: 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: rs10885406
rs10885406
0.925 0.120 10 113017965 intron variant A/G snv 0.55
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2008 2009
dbSNP: rs12573128
rs12573128
1.000 0.040 10 112971038 intron variant A/G snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 1.000 2 2012 2017
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 2 2007 2009
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: rs1006725
rs1006725
10 112970444 intron variant A/G snv 4.2E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs1006725
rs1006725
10 112970444 intron variant A/G snv 4.2E-03
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10885406
rs10885406
0.925 0.120 10 113017965 intron variant A/G snv 0.55
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs290489
rs290489
1.000 0.080 10 113147296 intron variant A/G snv 0.27
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7094463
rs7094463
10 112952224 intron variant A/G snv 0.57
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7100927
rs7100927
0.925 0.080 10 113036289 intron variant A/G snv 0.54
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs7100927
rs7100927
0.925 0.080 10 113036289 intron variant A/G snv 0.54
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs7100927
rs7100927
0.925 0.080 10 113036289 intron variant A/G snv 0.54
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2018 2018
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs7904519
rs7904519
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7906315
rs7906315
1.000 0.080 10 113127459 intron variant A/G snv 0.70
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4506565
rs4506565
0.790 0.280 10 112996282 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.870 0.900 10 2006 2020
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: rs4506565
rs4506565
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2016 2019