rs11196175
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11196175(C;C) |
Make rs11196175(C;T) |
Make rs11196175(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 112976855 |
Gene | TCF7L2 |
is a | snp |
is | mentioned by |
dbSNP | rs11196175 |
dbSNP (classic) | rs11196175 |
ClinGen | rs11196175 |
ebi | rs11196175 |
HLI | rs11196175 |
Exac | rs11196175 |
Gnomad | rs11196175 |
Varsome | rs11196175 |
LitVar | rs11196175 |
Map | rs11196175 |
PheGenI | rs11196175 |
Biobank | rs11196175 |
1000 genomes | rs11196175 |
hgdp | rs11196175 |
ensembl | rs11196175 |
geneview | rs11196175 |
scholar | rs11196175 |
rs11196175 | |
pharmgkb | rs11196175 |
gwascentral | rs11196175 |
openSNP | rs11196175 |
23andMe | rs11196175 |
SNPshot | rs11196175 |
SNPdbe | rs11196175 |
MSV3d | rs11196175 |
GWAS Ctlg | rs11196175 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28352326] Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study.