rs12526453
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12526453(C;C) |
Make rs12526453(C;G) |
Make rs12526453(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 12927312 |
Gene | PHACTR1 |
is a | snp |
is | mentioned by |
dbSNP | rs12526453 |
dbSNP (classic) | rs12526453 |
ClinGen | rs12526453 |
ebi | rs12526453 |
HLI | rs12526453 |
Exac | rs12526453 |
Gnomad | rs12526453 |
Varsome | rs12526453 |
LitVar | rs12526453 |
Map | rs12526453 |
PheGenI | rs12526453 |
Biobank | rs12526453 |
1000 genomes | rs12526453 |
hgdp | rs12526453 |
ensembl | rs12526453 |
geneview | rs12526453 |
scholar | rs12526453 |
rs12526453 | |
pharmgkb | rs12526453 |
gwascentral | rs12526453 |
openSNP | rs12526453 |
23andMe | rs12526453 |
SNPshot | rs12526453 |
SNPdbe | rs12526453 |
MSV3d | rs12526453 |
GWAS Ctlg | rs12526453 |
GMAF | 0.1905 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19198609] |
Trait | Myocardial infarction (early onset) |
Title | Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants |
Risk Allele | C |
P-val | 1E-9 |
Odds Ratio | 1.12 [1.08-1.17] |
GWAS snp | |
---|---|
PMID | [PMID 21378990] |
Trait | |
Title | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease |
Risk Allele | C |
P-val | 1E-9 |
Odds Ratio | 1.1000 [1.06-1.13] |
[PMID 22848412] Genetic Markers Enhance Coronary Risk Prediction in Men: The MORGAM Prospective Cohorts
[PMID 19956433] Genetics of coronary artery disease: focus on genome-wide association studies.
[PMID 20835900] Genetics of diabetes complications.
[PMID 22152955] Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.
[PMID 23561647] Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction