rs1005573
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1005573(C;C) |
| Make rs1005573(C;T) |
| Make rs1005573(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 21 |
| Position | 33026408 |
| Gene | OLIG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1005573 |
| dbSNP (classic) | rs1005573 |
| ClinGen | rs1005573 |
| ebi | rs1005573 |
| HLI | rs1005573 |
| Exac | rs1005573 |
| Gnomad | rs1005573 |
| Varsome | rs1005573 |
| LitVar | rs1005573 |
| Map | rs1005573 |
| PheGenI | rs1005573 |
| Biobank | rs1005573 |
| 1000 genomes | rs1005573 |
| hgdp | rs1005573 |
| ensembl | rs1005573 |
| geneview | rs1005573 |
| scholar | rs1005573 |
| rs1005573 | |
| pharmgkb | rs1005573 |
| gwascentral | rs1005573 |
| openSNP | rs1005573 |
| 23andMe | rs1005573 |
| SNPshot | rs1005573 |
| SNPdbe | rs1005573 |
| MSV3d | rs1005573 |
| GWAS Ctlg | rs1005573 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 30178266] Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic-Ischemic Encephalopathy.
