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rs290489

From SNPedia

Orientationplus
Stabilizedplus
Make rs290489(A;A)
Make rs290489(A;G)
Make rs290489(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position113147296
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs290489
ebirs290489
HLIrs290489
Exacrs290489
Varsomers290489
Maprs290489
PheGenIrs290489
hapmaprs290489
1000 genomesrs290489
hgdprs290489
ensemblrs290489
gopubmedrs290489
geneviewrs290489
scholarrs290489
googlers290489
pharmgkbrs290489
gwascentralrs290489
openSNPrs290489
23andMers290489
23andMe allrs290489
SNP Nexus

SNPshotrs290489
SNPdbers290489
MSV3drs290489
GWAS Ctlgrs290489
GMAF0.3655
Max Magnitude
? (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 19351735OA-icon.png] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.