Gene: TCF7L2 ×
Source: GWASCAT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007
dbSNP: rs7903146
rs7903146
TCF7L2
A 0.900 GeneticVariation GWASCAT A genome-wide association study of the metabolic syndrome in Indian Asian men. 20694148

2010
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007
dbSNP: rs7903146
rs7903146
TCF7L2
0.900 GeneticVariation GWASCAT A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. 17460697

2007
dbSNP: rs7903146
rs7903146
TCF7L2
0.900 GeneticVariation GWASCAT Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. 19056611

2009
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. 19401414

2009
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. 30470734

2018
dbSNP: rs7903146
rs7903146
TCF7L2
C 0.900 GeneticVariation GWASCAT Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. 30470734

2018
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. 31118516

2019
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Fine-mapping of the TCF7L2 locus suggested one type 2 diabetes association signal shared between Europeans and Africans (indexed by rs7903146) and a distinct African-specific signal (indexed by rs17746147). 31049640

2019
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. 19734900

2009
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). 28254843

2017
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018
dbSNP: rs117229942
rs117229942
TCF7L2
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018
dbSNP: rs4918796
rs4918796
TCF7L2
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007
dbSNP: rs34872471
rs34872471
TCF7L2
C 0.700 GeneticVariation GWASCAT Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes. 26818947

2016
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. 23209189

2013
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. 23300278

2013
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide association study identifies three novel loci for type 2 diabetes. 23945395

2014
dbSNP: rs4506565
rs4506565
TCF7L2
T 0.870 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs7901695
rs7901695
TCF7L2
0.900 GeneticVariation GWASCAT Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480

2014
dbSNP: rs7901695
rs7901695
TCF7L2
C 0.900 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926

2019
dbSNP: rs7903146
rs7903146
TCF7L2
T 0.900 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590

2017