rs944797
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs944797(C;C) |
| Make rs944797(C;T) |
| Make rs944797(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22115287 |
| Gene | CDKN2B-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs944797 |
| dbSNP (classic) | rs944797 |
| ClinGen | rs944797 |
| ebi | rs944797 |
| HLI | rs944797 |
| Exac | rs944797 |
| Gnomad | rs944797 |
| Varsome | rs944797 |
| LitVar | rs944797 |
| Map | rs944797 |
| PheGenI | rs944797 |
| Biobank | rs944797 |
| 1000 genomes | rs944797 |
| hgdp | rs944797 |
| ensembl | rs944797 |
| geneview | rs944797 |
| scholar | rs944797 |
| rs944797 | |
| pharmgkb | rs944797 |
| gwascentral | rs944797 |
| openSNP | rs944797 |
| 23andMe | rs944797 |
| SNPshot | rs944797 |
| SNPdbe | rs944797 |
| MSV3d | rs944797 |
| GWAS Ctlg | rs944797 |
| GMAF | 0.4913 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21971053 ]
|
| Trait | |
| Title | Genome-wide association study of coronary artery disease in the Japanese. |
| Risk Allele | C |
| P-val | 6E-16 |
| Odds Ratio | 1.2500 [1.18-1.31] |
[PMID 19463184] Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.
