rs740949
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs740949(A;A) |
| Make rs740949(A;G) |
| Make rs740949(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 7 |
| Position | 148808972 |
| Gene | EZH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs740949 |
| dbSNP (classic) | rs740949 |
| ClinGen | rs740949 |
| ebi | rs740949 |
| HLI | rs740949 |
| Exac | rs740949 |
| Gnomad | rs740949 |
| Varsome | rs740949 |
| LitVar | rs740949 |
| Map | rs740949 |
| PheGenI | rs740949 |
| Biobank | rs740949 |
| 1000 genomes | rs740949 |
| hgdp | rs740949 |
| ensembl | rs740949 |
| geneview | rs740949 |
| scholar | rs740949 |
| rs740949 | |
| pharmgkb | rs740949 |
| gwascentral | rs740949 |
| openSNP | rs740949 |
| 23andMe | rs740949 |
| SNPshot | rs740949 |
| SNPdbe | rs740949 |
| MSV3d | rs740949 |
| GWAS Ctlg | rs740949 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26552012] Chromatin remodeling gene EZH2 involved in the genetic etiology of autism in Chinese Han population
