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rs4132670

From SNPedia

Orientationminus
Stabilizedminus
Make rs4132670(C;C)
Make rs4132670(C;T)
Make rs4132670(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position113008012
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs4132670
ebirs4132670
HLIrs4132670
Exacrs4132670
Varsomers4132670
Maprs4132670
PheGenIrs4132670
hapmaprs4132670
1000 genomesrs4132670
hgdprs4132670
ensemblrs4132670
gopubmedrs4132670
geneviewrs4132670
scholarrs4132670
googlers4132670
pharmgkbrs4132670
gwascentralrs4132670
openSNPrs4132670
23andMers4132670
23andMe allrs4132670
SNP Nexus

SNPshotrs4132670
SNPdbers4132670
MSV3drs4132670
GWAS Ctlgrs4132670
GMAF0.314
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22402060OA-icon.png] Functional analysis of TCF7L2 genetic variants associated with type 2 diabetes


[PMID 19913122OA-icon.png] ATRIUM: testing untyped SNPs in case-control association studies with related individuals.


[PMID 20018041OA-icon.png] The effect of multiple genetic variants in predicting the risk of type 2 diabetes.