rs4132670
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4132670(C;C) |
| Make rs4132670(C;T) |
| Make rs4132670(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 113008012 |
| Gene | TCF7L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4132670 |
| dbSNP (classic) | rs4132670 |
| ClinGen | rs4132670 |
| ebi | rs4132670 |
| HLI | rs4132670 |
| Exac | rs4132670 |
| Gnomad | rs4132670 |
| Varsome | rs4132670 |
| LitVar | rs4132670 |
| Map | rs4132670 |
| PheGenI | rs4132670 |
| Biobank | rs4132670 |
| 1000 genomes | rs4132670 |
| hgdp | rs4132670 |
| ensembl | rs4132670 |
| geneview | rs4132670 |
| scholar | rs4132670 |
| rs4132670 | |
| pharmgkb | rs4132670 |
| gwascentral | rs4132670 |
| openSNP | rs4132670 |
| 23andMe | rs4132670 |
| SNPshot | rs4132670 |
| SNPdbe | rs4132670 |
| MSV3d | rs4132670 |
| GWAS Ctlg | rs4132670 |
| GMAF | 0.314 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22402060
] Functional analysis of TCF7L2 genetic variants associated with type 2 diabetes
[PMID 19913122] ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
[PMID 20018041] The effect of multiple genetic variants in predicting the risk of type 2 diabetes.
[PMID 32379818] Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose.
