rs290489
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs290489(A;A) |
Make rs290489(A;G) |
Make rs290489(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 113147296 |
Gene | TCF7L2 |
is a | snp |
is | mentioned by |
dbSNP | rs290489 |
dbSNP (classic) | rs290489 |
ClinGen | rs290489 |
ebi | rs290489 |
HLI | rs290489 |
Exac | rs290489 |
Gnomad | rs290489 |
Varsome | rs290489 |
LitVar | rs290489 |
Map | rs290489 |
PheGenI | rs290489 |
Biobank | rs290489 |
1000 genomes | rs290489 |
hgdp | rs290489 |
ensembl | rs290489 |
geneview | rs290489 |
scholar | rs290489 |
rs290489 | |
pharmgkb | rs290489 |
gwascentral | rs290489 |
openSNP | rs290489 |
23andMe | rs290489 |
SNPshot | rs290489 |
SNPdbe | rs290489 |
MSV3d | rs290489 |
GWAS Ctlg | rs290489 |
GMAF | 0.3655 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23558246] Impacts of TCF7L2 gene polymorphisms on the susceptibility of hepatogenous diabetes and hepatocellular carcinoma in cirrhotic patients
[PMID 19351735] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.