rs10885406
Orientation | plus |
Stabilized | plus |
Make rs10885406(A;A) |
Make rs10885406(A;G) |
Make rs10885406(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 113017965 |
Gene | TCF7L2 |
is a | snp |
is | mentioned by |
dbSNP | rs10885406 |
dbSNP (classic) | rs10885406 |
ClinGen | rs10885406 |
ebi | rs10885406 |
HLI | rs10885406 |
Exac | rs10885406 |
Gnomad | rs10885406 |
Varsome | rs10885406 |
LitVar | rs10885406 |
Map | rs10885406 |
PheGenI | rs10885406 |
Biobank | rs10885406 |
1000 genomes | rs10885406 |
hgdp | rs10885406 |
ensembl | rs10885406 |
geneview | rs10885406 |
scholar | rs10885406 |
rs10885406 | |
pharmgkb | rs10885406 |
gwascentral | rs10885406 |
openSNP | rs10885406 |
23andMe | rs10885406 |
SNPshot | rs10885406 |
SNPdbe | rs10885406 |
MSV3d | rs10885406 |
GWAS Ctlg | rs10885406 |
GMAF | 0.4256 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 17671651] Considered for type-2 diabetes in context with rs7903146 rs12255372 rs10885406.
[PMID 19183934] 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 19593725] 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.