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
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: rs117229942
rs117229942
1.000 0.080 10 112978018 intron variant C/T snv 5.8E-03
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 2 2018 2019
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
dbSNP: rs4918796
rs4918796
1.000 0.080 10 113120583 intron variant T/C snv 0.18
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 2 2018 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
0.700 1.000 2 2012 2012
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: 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: 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: rs11196169
rs11196169
10 112961478 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170
0.776 0.080 10 112962862 intron variant G/A;C snv
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
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
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
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170
0.776 0.080 10 112962862 intron variant G/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019