rs615552
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs615552(A;A) |
| Make rs615552(A;G) |
| Make rs615552(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 22026078 |
| Gene | CDKN2B-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs615552 |
| dbSNP (classic) | rs615552 |
| ClinGen | rs615552 |
| ebi | rs615552 |
| HLI | rs615552 |
| Exac | rs615552 |
| Gnomad | rs615552 |
| Varsome | rs615552 |
| LitVar | rs615552 |
| Map | rs615552 |
| PheGenI | rs615552 |
| Biobank | rs615552 |
| 1000 genomes | rs615552 |
| hgdp | rs615552 |
| ensembl | rs615552 |
| geneview | rs615552 |
| scholar | rs615552 |
| rs615552 | |
| pharmgkb | rs615552 |
| gwascentral | rs615552 |
| openSNP | rs615552 |
| 23andMe | rs615552 |
| SNPshot | rs615552 |
| SNPdbe | rs615552 |
| MSV3d | rs615552 |
| GWAS Ctlg | rs615552 |
| GMAF | 0.2172 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23361049
] Common genetic variants in the 9p21 region and their associations with multiple tumours
| GWAS snp | |
|---|---|
| PMID | [PMID 23793025]
|
| Trait | Migraine without aura |
| Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
| Risk Allele | C |
| P-val | 4E-6 |
| Odds Ratio | 1.10 [1.06-1.14] |
