rs10898459
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10898459(C;C) |
| Make rs10898459(C;T) |
| Make rs10898459(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 86261897 |
| Gene | EED |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10898459 |
| dbSNP (classic) | rs10898459 |
| ClinGen | rs10898459 |
| ebi | rs10898459 |
| HLI | rs10898459 |
| Exac | rs10898459 |
| Gnomad | rs10898459 |
| Varsome | rs10898459 |
| LitVar | rs10898459 |
| Map | rs10898459 |
| PheGenI | rs10898459 |
| Biobank | rs10898459 |
| 1000 genomes | rs10898459 |
| hgdp | rs10898459 |
| ensembl | rs10898459 |
| geneview | rs10898459 |
| scholar | rs10898459 |
| rs10898459 | |
| pharmgkb | rs10898459 |
| gwascentral | rs10898459 |
| openSNP | rs10898459 |
| 23andMe | rs10898459 |
| SNPshot | rs10898459 |
| SNPdbe | rs10898459 |
| MSV3d | rs10898459 |
| GWAS Ctlg | rs10898459 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25921222
] Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers
