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: 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: 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: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
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: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2018 2018