rs479526
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs479526(C;C) |
| Make rs479526(C;T) |
| Make rs479526(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 11617934 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs479526 |
| dbSNP (classic) | rs479526 |
| ClinGen | rs479526 |
| ebi | rs479526 |
| HLI | rs479526 |
| Exac | rs479526 |
| Gnomad | rs479526 |
| Varsome | rs479526 |
| LitVar | rs479526 |
| Map | rs479526 |
| PheGenI | rs479526 |
| Biobank | rs479526 |
| 1000 genomes | rs479526 |
| hgdp | rs479526 |
| ensembl | rs479526 |
| geneview | rs479526 |
| scholar | rs479526 |
| rs479526 | |
| pharmgkb | rs479526 |
| gwascentral | rs479526 |
| openSNP | rs479526 |
| 23andMe | rs479526 |
| SNPshot | rs479526 |
| SNPdbe | rs479526 |
| MSV3d | rs479526 |
| GWAS Ctlg | rs479526 |
| GMAF | 0.4821 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23738518 ]
|
| Trait | Reading and spelling |
| Title | A genome-wide association study for reading and language abilities in two population cohorts. |
| Risk Allele | T |
| P-val | 3E-6 |
| Odds Ratio | .09 [0.054-0.132] |
