rs12691
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs12691(C;C) |
Make rs12691(C;T) |
Make rs12691(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 33300221 |
Gene | CEBPA |
is a | snp |
is | mentioned by |
dbSNP | rs12691 |
dbSNP (classic) | rs12691 |
ClinGen | rs12691 |
ebi | rs12691 |
HLI | rs12691 |
Exac | rs12691 |
Gnomad | rs12691 |
Varsome | rs12691 |
LitVar | rs12691 |
Map | rs12691 |
PheGenI | rs12691 |
Biobank | rs12691 |
1000 genomes | rs12691 |
hgdp | rs12691 |
ensembl | rs12691 |
geneview | rs12691 |
scholar | rs12691 |
rs12691 | |
pharmgkb | rs12691 |
gwascentral | rs12691 |
openSNP | rs12691 |
23andMe | rs12691 |
SNPshot | rs12691 |
SNPdbe | rs12691 |
MSV3d | rs12691 |
GWAS Ctlg | rs12691 |
GMAF | 0.1442 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22269963] A gene variation (rs12691) in the CCAT/enhancer binding protein α modulates glucose metabolism in metabolic syndrome
[PMID 18765514] CCAAT/enhancer binding protein alpha (C/EBPalpha) in adipose tissue regulates genes in lipid and glucose metabolism and a genetic variation in C/EBPalpha is associated with serum levels of triglycerides.