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rs10885406

From SNPedia

Orientationplus
Stabilizedplus
Make rs10885406(A;A)
Make rs10885406(A;G)
Make rs10885406(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position113017965
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs10885406
ebirs10885406
HLIrs10885406
Exacrs10885406
Varsomers10885406
Maprs10885406
PheGenIrs10885406
hapmaprs10885406
1000 genomesrs10885406
hgdprs10885406
ensemblrs10885406
gopubmedrs10885406
geneviewrs10885406
scholarrs10885406
googlers10885406
pharmgkbrs10885406
gwascentralrs10885406
openSNPrs10885406
23andMers10885406
23andMe allrs10885406
SNP Nexus

SNPshotrs10885406
SNPdbers10885406
MSV3drs10885406
GWAS Ctlgrs10885406
GMAF0.4256
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 17671651OA-icon.png] Considered for type-2 diabetes in context with rs7903146 rs12255372 rs10885406.


[PMID 19183934OA-icon.png] TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study


[PMID 18239663] Effects of TCF7L2 polymorphisms on obesity in European populations.


[PMID 18839133] Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients.


[PMID 19593725OA-icon.png] Association of maternally inherited GNAS alleles with African-American male birth weight.


[PMID 22552033] Influence of dietary protein intake and glycemic index on the association between TCF7L2 HapA and weight gain.