rs2070531
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2070531(C;C) |
| Make rs2070531(C;T) |
| Make rs2070531(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 38822292 |
| Gene | ETS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2070531 |
| dbSNP (classic) | rs2070531 |
| ClinGen | rs2070531 |
| ebi | rs2070531 |
| HLI | rs2070531 |
| Exac | rs2070531 |
| Gnomad | rs2070531 |
| Varsome | rs2070531 |
| LitVar | rs2070531 |
| Map | rs2070531 |
| PheGenI | rs2070531 |
| Biobank | rs2070531 |
| 1000 genomes | rs2070531 |
| hgdp | rs2070531 |
| ensembl | rs2070531 |
| geneview | rs2070531 |
| scholar | rs2070531 |
| rs2070531 | |
| pharmgkb | rs2070531 |
| gwascentral | rs2070531 |
| openSNP | rs2070531 |
| 23andMe | rs2070531 |
| SNPshot | rs2070531 |
| SNPdbe | rs2070531 |
| MSV3d | rs2070531 |
| GWAS Ctlg | rs2070531 |
| GMAF | 0.2989 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23343470
] Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies
