rs6464926
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6464926(C;C) |
| Make rs6464926(C;T) |
| Make rs6464926(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 148821919 |
| Gene | EZH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6464926 |
| dbSNP (classic) | rs6464926 |
| ClinGen | rs6464926 |
| ebi | rs6464926 |
| HLI | rs6464926 |
| Exac | rs6464926 |
| Gnomad | rs6464926 |
| Varsome | rs6464926 |
| LitVar | rs6464926 |
| Map | rs6464926 |
| PheGenI | rs6464926 |
| Biobank | rs6464926 |
| 1000 genomes | rs6464926 |
| hgdp | rs6464926 |
| ensembl | rs6464926 |
| geneview | rs6464926 |
| scholar | rs6464926 |
| rs6464926 | |
| pharmgkb | rs6464926 |
| gwascentral | rs6464926 |
| openSNP | rs6464926 |
| 23andMe | rs6464926 |
| SNPshot | rs6464926 |
| SNPdbe | rs6464926 |
| MSV3d | rs6464926 |
| GWAS Ctlg | rs6464926 |
| GMAF | 0.4233 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22228224] EZH2 genetic variants affect risk of gastric cancer in the Chinese Han population
[PMID 26552012] Chromatin remodeling gene EZH2 involved in the genetic etiology of autism in Chinese Han population
