rs573687
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs573687(C;C) |
| Make rs573687(C;T) |
| Make rs573687(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22011643 |
| Gene | CDKN2B-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs573687 |
| dbSNP (classic) | rs573687 |
| ClinGen | rs573687 |
| ebi | rs573687 |
| HLI | rs573687 |
| Exac | rs573687 |
| Gnomad | rs573687 |
| Varsome | rs573687 |
| LitVar | rs573687 |
| Map | rs573687 |
| PheGenI | rs573687 |
| Biobank | rs573687 |
| 1000 genomes | rs573687 |
| hgdp | rs573687 |
| ensembl | rs573687 |
| geneview | rs573687 |
| scholar | rs573687 |
| rs573687 | |
| pharmgkb | rs573687 |
| gwascentral | rs573687 |
| openSNP | rs573687 |
| 23andMe | rs573687 |
| SNPshot | rs573687 |
| SNPdbe | rs573687 |
| MSV3d | rs573687 |
| GWAS Ctlg | rs573687 |
| GMAF | 0.1915 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23361049
] Common genetic variants in the 9p21 region and their associations with multiple tumours
