rs579459
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs579459(C;C) |
Make rs579459(C;T) |
Make rs579459(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 133278724 |
is a | snp |
is | mentioned by |
dbSNP | rs579459 |
dbSNP (classic) | rs579459 |
ClinGen | rs579459 |
ebi | rs579459 |
HLI | rs579459 |
Exac | rs579459 |
Gnomad | rs579459 |
Varsome | rs579459 |
LitVar | rs579459 |
Map | rs579459 |
PheGenI | rs579459 |
Biobank | rs579459 |
1000 genomes | rs579459 |
hgdp | rs579459 |
ensembl | rs579459 |
geneview | rs579459 |
scholar | rs579459 |
rs579459 | |
pharmgkb | rs579459 |
gwascentral | rs579459 |
openSNP | rs579459 |
23andMe | rs579459 |
SNPshot | rs579459 |
SNPdbe | rs579459 |
MSV3d | rs579459 |
GWAS Ctlg | rs579459 |
GMAF | 0.1887 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19729612] |
Trait | Serum soluble E-selectin |
Title | Genome-Wide Association Identifies the ABO Blood Group as a Major Locus Associated With Serum Levels of Soluble E-Selectin |
Risk Allele | C |
P-val | 1E-29 |
Odds Ratio | NR NR |
GWAS snp | |
---|---|
PMID | [PMID 20167578] |
Trait | Soluble levels of adhesion molecules |
Title | Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels |
Risk Allele | T |
P-val | 2E-41 |
Odds Ratio | 14.00 [12.04-15.96] % increase |
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 | 4E-14 |
Odds Ratio | 1.1000 [1.07-1.13] |
[PMID 22010135] Association of Variation at the ABO Locus with Circulating Levels of sICAM-1, sP-selectin and sE-selectin: A Meta-Analysis
GWAS snp | |
---|---|
PMID | [PMID 22001757] |
Trait | |
Title | Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. |
Risk Allele | T |
P-val | 3E-123 |
Odds Ratio | 8.8000 None |
GWAS snp | |
---|---|
PMID | [PMID 23222517] |
Trait | Red blood cell traits |
Title | Seventy-five genetic loci influencing the human red blood cell. |
Risk Allele | T |
P-val | 9E-18 |
Odds Ratio | .02 [0.015-0.027] unit increase |
[PMID 23161703] Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
GWAS snp | |
---|---|
PMID | [PMID 24262325] |
Trait | Coronary artery disease |
Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
Risk Allele | C |
P-val | 2E-7 |
Odds Ratio | 1.10 [1.06-1.14] |
GWAS snp | |
---|---|
PMID | [PMID 24586186] |
Trait | Urinary metabolites (H-NMR features) |
Title | Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. |
Risk Allele | T |
P-val | 1E-28 |
Odds Ratio | .49 [NR] unit increase |
GWAS snp | |
---|---|
PMID | [PMID 24816252] |
Trait | Blood metabolite ratios |
Title | An atlas of genetic influences on human blood metabolites. |
Risk Allele | T |
P-val | 1E-28 |
Odds Ratio | .12 [0.1-0.15] unit decrease |
[PMID 24251769] LDL-c-linked SNPs are associated with LDL-c and myocardial infarction despite lipid-lowering therapy in patients with established vascular disease
[PMID 26413716] A GWAS Study on Liver Function Test Using eMERGE Network Participants
[PMID 29390587] Prospective association of a genetic risk score with major adverse cardiovascular events in patients with coronary artery disease.