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
Latent autoimmune diabetes mellitus in adult
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.050 1.000 5 2008 2019
dbSNP: rs10885409
rs10885409
1.000 0.080 10 113048313 intron variant T/C snv 0.54
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.720 1.000 4 2007 2015
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
Malignant neoplasm 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
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 4 2014 2019
dbSNP: rs34872471
rs34872471
1.000 0.080 10 112994312 intron variant T/C snv 0.29
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 4 2014 2018
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: rs7895340
rs7895340
0.851 0.160 10 113041766 intron variant G/A snv 0.53
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.040 0.500 4 2007 2013
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.040 0.750 4 2007 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
Nutritional and Metabolic Diseases 0.040 0.750 4 2006 2017
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: rs11196236
rs11196236
0.925 0.160 10 113127963 intron variant T/C snv 0.16
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.030 0.333 3 2009 2013
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.030 1.000 3 2016 2019
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
Malignant neoplasm of colon and/or rectum
0.030 1.000 3 2016 2019
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.030 1.000 3 2014 2015
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
Nutritional and Metabolic Diseases 0.030 1.000 3 2006 2011
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.030 0.667 3 2009 2018
dbSNP: rs7901695
rs7901695
0.851 0.160 10 112994329 intron variant T/C snv 0.34
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.030 1.000 3 2011 2017
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.030 1.000 3 2014 2018
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.030 1.000 3 2008 2018