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: rs3814570
rs3814570 		0.925 0.040 10 112948751 upstream gene variant C/T snv 0.23
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3814570
rs3814570 		0.925 0.040 10 112948751 upstream gene variant C/T snv 0.23
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs557826746
rs557826746 		1.000 0.080 10 112950901 missense variant G/C snv 4.0E-06
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
TROPICAL CALCIFIC PANCREATITIS 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008
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: rs1157868044
rs1157868044 		1.000 0.080 10 112951246 missense variant G/A snv
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 2015 2015
dbSNP: rs7094463
rs7094463 		10 112952224 intron variant A/G snv 0.57
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7094871
rs7094871 		1.000 0.080 10 112952395 intron variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2104598
rs2104598 		10 112955839 intron variant G/A snv 0.55
CUI: C0596887
Disease: mathematical ability
mathematical ability 		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
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
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170 		0.776 0.080 10 112962862 intron variant G/A;C snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
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
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2014 2019