Rs290481

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Orientationminus
Make rs290481(A;A)
Make rs290481(A;G)
Make rs290481(G;G)
ReferenceGRCh37 37.1/131
Chromosome10
Position114923825
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs290481
PheGenIrs290481
nextbiors290481
hapmaprs290481
1000 genomesrs290481
hgdprs290481
ensemblrs290481
gopubmedrs290481
geneviewrs290481
scholarrs290481
googlers290481
pharmgkbrs290481
gwascentralrs290481
openSNPrs290481
23andMers290481
23andMe allrs290481
SNP Nexus

SNPshotrs290481
SNPdbers290481
MSV3drs290481
GMAF0.3017
Max Magnitude
? (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 22361517OA-icon.png] 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 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

[PMID 19351735OA-icon.png] 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