rs461155
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs461155(A;A) |
| Make rs461155(A;G) |
| Make rs461155(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 38819714 |
| Gene | ETS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs461155 |
| dbSNP (classic) | rs461155 |
| ClinGen | rs461155 |
| ebi | rs461155 |
| HLI | rs461155 |
| Exac | rs461155 |
| Gnomad | rs461155 |
| Varsome | rs461155 |
| LitVar | rs461155 |
| Map | rs461155 |
| PheGenI | rs461155 |
| Biobank | rs461155 |
| 1000 genomes | rs461155 |
| hgdp | rs461155 |
| ensembl | rs461155 |
| geneview | rs461155 |
| scholar | rs461155 |
| rs461155 | |
| pharmgkb | rs461155 |
| gwascentral | rs461155 |
| openSNP | rs461155 |
| 23andMe | rs461155 |
| SNPshot | rs461155 |
| SNPdbe | rs461155 |
| MSV3d | rs461155 |
| GWAS Ctlg | rs461155 |
| GMAF | 0.3636 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23343470
] Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies
