rs5987201
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs5987201(C;T) |
| Make rs5987201(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 154064591 |
| Gene | MECP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5987201 |
| dbSNP (classic) | rs5987201 |
| ClinGen | rs5987201 |
| ebi | rs5987201 |
| HLI | rs5987201 |
| Exac | rs5987201 |
| Gnomad | rs5987201 |
| Varsome | rs5987201 |
| LitVar | rs5987201 |
| Map | rs5987201 |
| PheGenI | rs5987201 |
| Biobank | rs5987201 |
| 1000 genomes | rs5987201 |
| hgdp | rs5987201 |
| ensembl | rs5987201 |
| geneview | rs5987201 |
| scholar | rs5987201 |
| rs5987201 | |
| pharmgkb | rs5987201 |
| gwascentral | rs5987201 |
| openSNP | rs5987201 |
| 23andMe | rs5987201 |
| SNPshot | rs5987201 |
| SNPdbe | rs5987201 |
| MSV3d | rs5987201 |
| GWAS Ctlg | rs5987201 |
| GMAF | 0.07739 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23444193
] New insight on the Xq28 association with systemic sclerosis
[PMID 18320046] Common variants within MECP2 confer risk of systemic lupus erythematosus.
[PMID 19333917] Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to lupus and differential gene expression in patients with systemic lupus erythematosus.
