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
google	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