rs290481
Orientation | minus |
Stabilized | minus |
Make rs290481(A;A) |
Make rs290481(A;G) |
Make rs290481(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 113164066 |
Gene | TCF7L2 |
is a | snp |
is | mentioned by |
dbSNP | rs290481 |
dbSNP (classic) | rs290481 |
ClinGen | rs290481 |
ebi | rs290481 |
HLI | rs290481 |
Exac | rs290481 |
Gnomad | rs290481 |
Varsome | rs290481 |
LitVar | rs290481 |
Map | rs290481 |
PheGenI | rs290481 |
Biobank | rs290481 |
1000 genomes | rs290481 |
hgdp | rs290481 |
ensembl | rs290481 |
geneview | rs290481 |
scholar | rs290481 |
rs290481 | |
pharmgkb | rs290481 |
gwascentral | rs290481 |
openSNP | rs290481 |
23andMe | rs290481 |
SNPshot | rs290481 |
SNPdbe | rs290481 |
MSV3d | rs290481 |
GWAS Ctlg | rs290481 |
GMAF | 0.3017 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19806338] TCF7L2 genetic variants and progression to diabetes in the Chinese population: pleiotropic effects on insulin secretion and insulin resistance
[PMID 22361517] Genetic determinants of the ankle-brachial index: A meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium
[PMID 16385451] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
[PMID 19351735] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.
[PMID 21115178] Pleiotropic effects of TCF7L2 gene variants and its modulation in the metabolic syndrome: from the LIPGENE study.
[PMID 23558246] Impacts of TCF7L2 gene polymorphisms on the susceptibility of hepatogenous diabetes and hepatocellular carcinoma in cirrhotic patients
[PMID 24468095] Genetic variants for type 2 diabetes and new-onset cancer in Chinese with type 2 diabetes
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d