Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7903146
rs7903146
TCF7L2
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 		0.900 0.953 28 2006 2020
dbSNP: rs7901695
rs7901695
TCF7L2
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 		0.900 1.000 3 2006 2020
dbSNP: rs4506565
rs4506565
TCF7L2
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 		0.870 0.900 1 2006 2020
dbSNP: rs7903146
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.870 0.875 1 2008 2018
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.820 0.833 4 2014 2019
dbSNP: rs7903146
rs7903146
TCF7L2
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: rs4506565
rs4506565
TCF7L2
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 3 2010 2019
dbSNP: rs7903146
rs7903146
TCF7L2
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 2 2009 2019
dbSNP: rs11196174
rs11196174
TCF7L2
1.000 0.080 10 112974337 intron variant A/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.800 1.000 1 2013 2013
dbSNP: rs12243326
rs12243326
TCF7L2
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: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2016
dbSNP: rs7903146
rs7903146
TCF7L2
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: rs7904519
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.710 1.000 3 2013 2018
dbSNP: rs12772424
rs12772424
TCF7L2
1.000 0.040 10 113120792 intron variant A/T snv 0.57
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.710 1.000 1 2014 2016
dbSNP: rs7903146
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.710 1.000 1 2011 2018
dbSNP: rs7903146
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.710 1.000 1 2019 2020
dbSNP: rs11196172
rs11196172
TCF7L2
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 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 4 2014 2019
dbSNP: rs11196172
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 4 2014 2019
dbSNP: rs34872471
rs34872471
TCF7L2
1.000 0.080 10 112994312 intron variant T/C snv 0.29
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 4 2014 2018