rs17098356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17098356(G;G) |
| Make rs17098356(G;T) |
| Make rs17098356(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 61432121 |
| Gene | PRKCH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17098356 |
| dbSNP (classic) | rs17098356 |
| ClinGen | rs17098356 |
| ebi | rs17098356 |
| HLI | rs17098356 |
| Exac | rs17098356 |
| Gnomad | rs17098356 |
| Varsome | rs17098356 |
| LitVar | rs17098356 |
| Map | rs17098356 |
| PheGenI | rs17098356 |
| Biobank | rs17098356 |
| 1000 genomes | rs17098356 |
| hgdp | rs17098356 |
| ensembl | rs17098356 |
| geneview | rs17098356 |
| scholar | rs17098356 |
| rs17098356 | |
| pharmgkb | rs17098356 |
| gwascentral | rs17098356 |
| openSNP | rs17098356 |
| 23andMe | rs17098356 |
| SNPshot | rs17098356 |
| SNPdbe | rs17098356 |
| MSV3d | rs17098356 |
| GWAS Ctlg | rs17098356 |
| GMAF | 0.3214 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | |
| P-val | 6E-6 |
| Odds Ratio | NR NR |
