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rs10749127

From SNPedia

Orientationplus
Stabilizedplus
Make rs10749127(C;C)
Make rs10749127(C;T)
Make rs10749127(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position113089594
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs10749127
dbSNP (classic)rs10749127
ClinGenrs10749127
ebirs10749127
HLIrs10749127
Exacrs10749127
Gnomadrs10749127
Varsomers10749127
LitVarrs10749127
Maprs10749127
PheGenIrs10749127
Biobankrs10749127
1000 genomesrs10749127
hgdprs10749127
ensemblrs10749127
geneviewrs10749127
scholarrs10749127
googlers10749127
pharmgkbrs10749127
gwascentralrs10749127
openSNPrs10749127
23andMers10749127
SNPshotrs10749127
SNPdbers10749127
MSV3drs10749127
GWAS Ctlgrs10749127
GMAF0.2805
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19509102] Genetic Variants of TCF7L2 are Associated with Insulin Resistance and Related Metabolic Phenotypes in Taiwanese Adolescents and Caucasian Young Adults


[PMID 25678841OA-icon.png] Genetic Interaction Analysis of TCF7L2 for Biochemical Recurrence after Radical Prostatectomy in Localized Prostate Cancer