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: rs575072438
rs575072438 		1.000 0.040 10 113152371 synonymous variant C/T snv 2.8E-05 2.1E-05
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs766727892
rs766727892 		0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06
CUI: C4086152
Disease: Childhood Astrocytoma
Childhood Astrocytoma 		Neoplasms 0.010 1.000 1 2002 2002
dbSNP: rs766727892
rs766727892 		0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		Neoplasms; Nervous System Diseases 0.010 < 0.001 1 2002 2002
dbSNP: rs766727892
rs766727892 		0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		Neoplasms 0.010 1.000 1 2002 2002
dbSNP: rs768298443
rs768298443 		1.000 0.040 10 112950932 missense variant C/A snv 4.1E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs768298443
rs768298443 		1.000 0.040 10 112950932 missense variant C/A snv 4.1E-06
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs780571021
rs780571021 		1.000 0.040 10 113146069 missense variant G/C;T snv 4.0E-06; 8.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs780571021
rs780571021 		1.000 0.040 10 113146069 missense variant G/C;T snv 4.0E-06; 8.0E-06
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma 		Neoplasms 0.010 1.000 1 2019 2019
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: rs34872471
rs34872471 		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 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 4 2014 2018
dbSNP: rs117229942
rs117229942 		1.000 0.080 10 112978018 intron variant C/T snv 5.8E-03
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 2 2018 2019
dbSNP: rs3814573
rs3814573 		1.000 0.080 10 113138334 intron variant T/C snv 0.71
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2007 2008
dbSNP: rs4918796
rs4918796 		1.000 0.080 10 113120583 intron variant T/C snv 0.18
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 2 2018 2019
dbSNP: rs10885405
rs10885405 		1.000 0.080 10 113017911 intron variant C/T snv 0.53
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10885409
rs10885409 		1.000 0.080 10 113048313 intron variant T/C snv 0.54
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2018 2018
dbSNP: rs10885409
rs10885409 		1.000 0.080 10 113048313 intron variant T/C snv 0.54
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10885421
rs10885421 		1.000 0.080 10 113156827 intron variant G/T snv 0.52
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019