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rs1255372

From SNPedia

Orientationplus
Stabilizedplus
Make rs1255372(C;C)
Make rs1255372(C;T)
Make rs1255372(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position42496332
GeneLOC84856
is asnp
is mentioned by
dbSNPrs1255372
ebirs1255372
HLIrs1255372
Exacrs1255372
Varsomers1255372
Maprs1255372
PheGenIrs1255372
hapmaprs1255372
1000 genomesrs1255372
hgdprs1255372
ensemblrs1255372
gopubmedrs1255372
geneviewrs1255372
scholarrs1255372
googlers1255372
pharmgkbrs1255372
gwascentralrs1255372
openSNPrs1255372
23andMers1255372
23andMe allrs1255372
SNP Nexus

SNPshotrs1255372
SNPdbers1255372
MSV3drs1255372
GWAS Ctlgrs1255372
GMAF0.3039
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 17340123] rs12255372, rs7903146, rs7901695 and rs11196205 associated with type-2 diabetes


[PMID 20028944OA-icon.png] Gene variants of TCF7L2 influence weight loss and body composition during lifestyle intervention in a risk population for type 2 diabetes


[PMID 17661009OA-icon.png] Impaired glucagon-like peptide-1-induced insulin secretion in carriers of transcription factor 7-like 2 (TCF7L2) gene polymorphisms.