rs290487
Orientation | plus |
Stabilized | plus |
Make rs290487(C;C) |
Make rs290487(C;T) |
Make rs290487(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 113149972 |
Gene | TCF7L2 |
is a | snp |
is | mentioned by |
dbSNP | rs290487 |
dbSNP (classic) | rs290487 |
ClinGen | rs290487 |
ebi | rs290487 |
HLI | rs290487 |
Exac | rs290487 |
Gnomad | rs290487 |
Varsome | rs290487 |
LitVar | rs290487 |
Map | rs290487 |
PheGenI | rs290487 |
Biobank | rs290487 |
1000 genomes | rs290487 |
hgdp | rs290487 |
ensembl | rs290487 |
geneview | rs290487 |
scholar | rs290487 |
rs290487 | |
pharmgkb | rs290487 |
gwascentral | rs290487 |
openSNP | rs290487 |
23andMe | rs290487 |
SNPshot | rs290487 |
SNPdbe | rs290487 |
MSV3d | rs290487 |
GWAS Ctlg | rs290487 |
GMAF | 0.2746 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19509102] Genetic Variants of TCF7L2 are Associated with Insulin Resistance and Related Metabolic Phenotypes in Taiwanese Adolescents and Caucasian Young Adults
[PMID 19718565] Genetic variants of cyclin-dependent kinase 5 regulatory subunit associated protein 1-like 1 and transcription factor 7-like 2 are not associated with polycystic ovary syndrome in Chinese women
[PMID 20054294] KCNJ11 Lys23Glu and TCF7L2 rs290487(C/T) Polymorphisms Affect Therapeutic Efficacy of Repaglinide in Chinese Patients With Type 2 Diabetes
[PMID 22296403] Common variants of transcription factor 7-like 2 (TCF7L2) are associated with reduced insulin secretion in women with polycystic ovary syndrome
[PMID 17579206] Association study of the genetic polymorphisms of the transcription factor 7-like 2 (TCF7L2) gene and type 2 diabetes in the Chinese population.
[PMID 18097733] Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects.
[PMID 18493736] Exon sequencing and association analysis of polymorphisms in TCF7L2 with type 2 diabetes in a Chinese population.
[PMID 19482368] Meta-analysis of the association between SNPs in TCF7L2 and type 2 diabetes in East Asian population.
[PMID 20161779] Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort.
[PMID 23041303] Association between donor and recipient TCF7L2 gene polymorphisms and the risk of new-onset diabetes mellitus after liver transplantation in a Han Chinese population
[PMID 23536853] Association of rs7903146 (IVS3C/T) and rs290487 (IVS3C/T) Polymorphisms in TCF7L2 with Type 2 Diabetes in 9,619 Han Chinese Population
[PMID 23311683] Meta-analysis of associations between TCF7L2 polymorphisms and risk of type 2 diabetes mellitus in the Chinese population
[PMID 23558246] Impacts of TCF7L2 gene polymorphisms on the susceptibility of hepatogenous diabetes and hepatocellular carcinoma in cirrhotic patients
[PMID 23188737] TCF7L2 gene polymorphisms and type 2 diabetes risk: a comprehensive and updated meta-analysis involving 121,174 subjects
[PMID 23010200] Association of TCF7L2 gene polymorphisms with type 2 diabetes mellitus in Han Chinese population: a meta-analysis.
[PMID 24002895] Rs290487 of TCF7L2 gene is not associated with type 2 diabetes in Chinese Han population: a case control study and meta-analysis
[PMID 25185411] Association of rs7903146, rs12255372, and rs290487 polymorphisms in TCF7L2 gene with type 2 diabetes in an Iranian Kurdish ethnic group
[PMID 26109524] Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese
[PMID 33419631] Association of TCF7L2 gene polymorphisms, methylation, and gene-environment interaction with type 2 diabetes mellitus risk: A nested case-control study in the Rural Chinese Cohort Study.