rs290227
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs290227(C;C) |
| Make rs290227(C;T) |
| Make rs290227(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 90874382 |
| Gene | SYK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs290227 |
| dbSNP (classic) | rs290227 |
| ClinGen | rs290227 |
| ebi | rs290227 |
| HLI | rs290227 |
| Exac | rs290227 |
| Gnomad | rs290227 |
| Varsome | rs290227 |
| LitVar | rs290227 |
| Map | rs290227 |
| PheGenI | rs290227 |
| Biobank | rs290227 |
| 1000 genomes | rs290227 |
| hgdp | rs290227 |
| ensembl | rs290227 |
| geneview | rs290227 |
| scholar | rs290227 |
| rs290227 | |
| pharmgkb | rs290227 |
| gwascentral | rs290227 |
| openSNP | rs290227 |
| 23andMe | rs290227 |
| SNPshot | rs290227 |
| SNPdbe | rs290227 |
| MSV3d | rs290227 |
| GWAS Ctlg | rs290227 |
| GMAF | 0.3866 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23480133] Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia
