rs9632884
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9632884(C;C) |
Make rs9632884(C;G) |
Make rs9632884(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 22072302 |
Gene | CDKN2B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs9632884 |
dbSNP (classic) | rs9632884 |
ClinGen | rs9632884 |
ebi | rs9632884 |
HLI | rs9632884 |
Exac | rs9632884 |
Gnomad | rs9632884 |
Varsome | rs9632884 |
LitVar | rs9632884 |
Map | rs9632884 |
PheGenI | rs9632884 |
Biobank | rs9632884 |
1000 genomes | rs9632884 |
hgdp | rs9632884 |
ensembl | rs9632884 |
geneview | rs9632884 |
scholar | rs9632884 |
rs9632884 | |
pharmgkb | rs9632884 |
gwascentral | rs9632884 |
openSNP | rs9632884 |
23andMe | rs9632884 |
SNPshot | rs9632884 |
SNPdbe | rs9632884 |
MSV3d | rs9632884 |
GWAS Ctlg | rs9632884 |
GMAF | 0.332 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
Rs9632884 | |
---|---|
PubMed | [PMID 17478681] |
Affy Probeset | SNP_A-2063543 |
Affy Orientation | same |
On GW 5.0 | 1 |
Alleles A/B | C/G |
Ancestral | C |
Population | CEU |
Allele | C |
Case Freq. | |
Control Freq. | |
Odds Ratio Het | 1.30 |
Odds Ratio Hom | 1.54 |
Odds Ratio All | 1.23 |
Disease | Coronary artery disease (CAD) |
rs9632884 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (CG) and 1.54 times for homozygotes (CC) [PMID 17478681]
[PMID 30898706] Association of lncRNA polymorphisms with triglyceride and total cholesterol levels among myocardial infarction patients in Chinese population.
[PMID 32293292] Susceptible gene polymorphism in patients with three-vessel coronary artery disease.