TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.820 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.820 GeneticVariation GWASDB Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009404
Disease:
Colorectal Neoplasms
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0007102
Disease:
Malignant tumor of colon
A 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.820 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009404
Disease:
Colorectal Neoplasms
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0007102
Disease:
Malignant tumor of colon
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
A 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.820 GeneticVariation BEFREE The results indicated that the TCF7L2 rs11196172 polymorphism increases the risk of CRC independently, with no evidence of an interaction with diabetes or obesity. 27792933 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE The results indicated that the TCF7L2 rs11196172 polymorphism increases the risk of CRC independently, with no evidence of an interaction with diabetes or obesity. 27792933 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE The results indicated that the TCF7L2 rs11196172 polymorphism increases the risk of CRC independently, with no evidence of an interaction with diabetes or obesity. 27792933 2016
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.820 GeneticVariation BEFREE Cumulative epidemiological evidence of an association was graded as strong for rs7903146 [odds ratio (OR) = 1.05, p = 4.13 × 10<sup>-5</sup> ] and rs7904519 (OR = 1.07, p = 2.02 × 10<sup>-14</sup> ) in breast cancer, rs11196172 (OR = 1.11, p = 2.22 × 10<sup>-16</sup> ), rs12241008 (OR = 1.13, p = 1.36 × 10<sup>-10</sup> ) and rs10506868 (OR = 1.10, p = 3.98 × 10<sup>-9</sup> ) in colorectal cancer, rs7086803 in lung cancer (OR = 1.30, p = 3.54 × 10<sup>-18</sup> ) and rs11196067 (OR = 1.18, p = 3.59 × 10<sup>-13</sup> ) in glioma, moderate for rs12255372 (OR = 1.12, p = 2.52 × 10<sup>-4</sup> ) in breast cancer and weak for rs7903146 (OR = 1.11, p = 0.007) in colorectal cancer. 28949031 2018
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE Cumulative epidemiological evidence of an association was graded as strong for rs7903146 [odds ratio (OR) = 1.05, p = 4.13 × 10<sup>-5</sup> ] and rs7904519 (OR = 1.07, p = 2.02 × 10<sup>-14</sup> ) in breast cancer, rs11196172 (OR = 1.11, p = 2.22 × 10<sup>-16</sup> ), rs12241008 (OR = 1.13, p = 1.36 × 10<sup>-10</sup> ) and rs10506868 (OR = 1.10, p = 3.98 × 10<sup>-9</sup> ) in colorectal cancer, rs7086803 in lung cancer (OR = 1.30, p = 3.54 × 10<sup>-18</sup> ) and rs11196067 (OR = 1.18, p = 3.59 × 10<sup>-13</sup> ) in glioma, moderate for rs12255372 (OR = 1.12, p = 2.52 × 10<sup>-4</sup> ) in breast cancer and weak for rs7903146 (OR = 1.11, p = 0.007) in colorectal cancer. 28949031 2018
dbSNP: rs11196172
rs11196172
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0017638
Disease:
Glioma
0.010 GeneticVariation BEFREE Cumulative epidemiological evidence of an association was graded as strong for rs7903146 [odds ratio (OR) = 1.05, p = 4.13 × 10<sup>-5</sup> ] and rs7904519 (OR = 1.07, p = 2.02 × 10<sup>-14</sup> ) in breast cancer, rs11196172 (OR = 1.11, p = 2.22 × 10<sup>-16</sup> ), rs12241008 (OR = 1.13, p = 1.36 × 10<sup>-10</sup> ) and rs10506868 (OR = 1.10, p = 3.98 × 10<sup>-9</sup> ) in colorectal cancer, rs7086803 in lung cancer (OR = 1.30, p = 3.54 × 10<sup>-18</sup> ) and rs11196067 (OR = 1.18, p = 3.59 × 10<sup>-13</sup> ) in glioma, moderate for rs12255372 (OR = 1.12, p = 2.52 × 10<sup>-4</sup> ) in breast cancer and weak for rs7903146 (OR = 1.11, p = 0.007) in colorectal cancer. 28949031 2018