rs2734647
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2734647(C;C) |
| Make rs2734647(C;T) |
| Make rs2734647(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 154026729 |
| Gene | MECP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2734647 |
| dbSNP (classic) | rs2734647 |
| ClinGen | rs2734647 |
| ebi | rs2734647 |
| HLI | rs2734647 |
| Exac | rs2734647 |
| Gnomad | rs2734647 |
| Varsome | rs2734647 |
| LitVar | rs2734647 |
| Map | rs2734647 |
| PheGenI | rs2734647 |
| Biobank | rs2734647 |
| 1000 genomes | rs2734647 |
| hgdp | rs2734647 |
| ensembl | rs2734647 |
| geneview | rs2734647 |
| scholar | rs2734647 |
| rs2734647 | |
| pharmgkb | rs2734647 |
| gwascentral | rs2734647 |
| openSNP | rs2734647 |
| 23andMe | rs2734647 |
| SNPshot | rs2734647 |
| SNPdbe | rs2734647 |
| MSV3d | rs2734647 |
| GWAS Ctlg | rs2734647 |
| GMAF | 0.3277 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24043878
] Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese
[PMID 18454203] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
