rs878949
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs878949(C;C) |
| Make rs878949(C;T) |
| Make rs878949(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 21900598 |
| Gene | HSPG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs878949 |
| dbSNP (classic) | rs878949 |
| ClinGen | rs878949 |
| ebi | rs878949 |
| HLI | rs878949 |
| Exac | rs878949 |
| Gnomad | rs878949 |
| Varsome | rs878949 |
| LitVar | rs878949 |
| Map | rs878949 |
| PheGenI | rs878949 |
| Biobank | rs878949 |
| 1000 genomes | rs878949 |
| hgdp | rs878949 |
| ensembl | rs878949 |
| geneview | rs878949 |
| scholar | rs878949 |
| rs878949 | |
| pharmgkb | rs878949 |
| gwascentral | rs878949 |
| openSNP | rs878949 |
| 23andMe | rs878949 |
| SNPshot | rs878949 |
| SNPdbe | rs878949 |
| MSV3d | rs878949 |
| GWAS Ctlg | rs878949 |
| GMAF | 0.3636 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21808285] Support for association of HSPG2 with tardive dyskinesia in Caucasian populations
