rs1537378
| Orientation | minus |
| Stabilized | minus |
| Make rs1537378(C;C) |
| Make rs1537378(C;T) |
| Make rs1537378(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22061615 |
| Gene | CDKN2B-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1537378 |
| dbSNP (classic) | rs1537378 |
| ClinGen | rs1537378 |
| ebi | rs1537378 |
| HLI | rs1537378 |
| Exac | rs1537378 |
| Gnomad | rs1537378 |
| Varsome | rs1537378 |
| LitVar | rs1537378 |
| Map | rs1537378 |
| PheGenI | rs1537378 |
| Biobank | rs1537378 |
| 1000 genomes | rs1537378 |
| hgdp | rs1537378 |
| ensembl | rs1537378 |
| geneview | rs1537378 |
| scholar | rs1537378 |
| rs1537378 | |
| pharmgkb | rs1537378 |
| gwascentral | rs1537378 |
| openSNP | rs1537378 |
| 23andMe | rs1537378 |
| SNPshot | rs1537378 |
| SNPdbe | rs1537378 |
| MSV3d | rs1537378 |
| GWAS Ctlg | rs1537378 |
| GMAF | 0.2002 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19475673
] Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke
[PMID 19926059] No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents
[PMID 21511257] The chromosome 9p21 region and myocardial infarction in a European population
[PMID 18362232] Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
[PMID 19359634] Update on the genetics of stroke and cerebrovascular disease 2008.
[PMID 20395606] Chromosome 9p21 in ischemic stroke: population structure and meta-analysis.
[PMID 25665551] Chromosome 9p21.3 Variants Are Associated with Cerebral Infarction in Chinese Population
[PMID 25724239] Sequence Variants on Chromosome 9p21 are Associated with Ischemic Stroke and the Lipids Level in Chinese Han Population
[PMID 29773352] The ANRIL Genetic Variants and Their Interactions with Environmental Risk Factors on Atherothrombotic Stroke in a Han Chinese Population.
