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rs17747324

From SNPedia

Orientationplus
Stabilizedplus
Make rs17747324(C;C)
Make rs17747324(C;T)
Make rs17747324(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position112992744
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs17747324
ebirs17747324
HLIrs17747324
Exacrs17747324
Varsomers17747324
Maprs17747324
PheGenIrs17747324
hapmaprs17747324
1000 genomesrs17747324
hgdprs17747324
ensemblrs17747324
gopubmedrs17747324
geneviewrs17747324
scholarrs17747324
googlers17747324
pharmgkbrs17747324
gwascentralrs17747324
openSNPrs17747324
23andMers17747324
23andMe allrs17747324
SNP Nexus

SNPshotrs17747324
SNPdbers17747324
MSV3drs17747324
GWAS Ctlgrs17747324
GMAF0.1276
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 19351735OA-icon.png] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.