rs886126
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs886126(C;C) |
Make rs886126(C;T) |
Make rs886126(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 111241410 |
Gene | CUX2 |
is a | snp |
is | mentioned by |
dbSNP | rs886126 |
dbSNP (classic) | rs886126 |
ClinGen | rs886126 |
ebi | rs886126 |
HLI | rs886126 |
Exac | rs886126 |
Gnomad | rs886126 |
Varsome | rs886126 |
LitVar | rs886126 |
Map | rs886126 |
PheGenI | rs886126 |
Biobank | rs886126 |
1000 genomes | rs886126 |
hgdp | rs886126 |
ensembl | rs886126 |
geneview | rs886126 |
scholar | rs886126 |
rs886126 | |
pharmgkb | rs886126 |
gwascentral | rs886126 |
openSNP | rs886126 |
23andMe | rs886126 |
SNPshot | rs886126 |
SNPdbe | rs886126 |
MSV3d | rs886126 |
GWAS Ctlg | rs886126 |
GMAF | 0.4463 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23364394] |
Trait | Coronary heart disease |
Title | A genome-wide association study of a coronary artery disease risk variant. |
Risk Allele | T |
P-val | 1E-6 |
Odds Ratio | 1.14 [1.08-1.20] |