rs4751178
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4751178(A;A) |
| Make rs4751178(A;G) |
| Make rs4751178(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 130193981 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4751178 |
| dbSNP (classic) | rs4751178 |
| ClinGen | rs4751178 |
| ebi | rs4751178 |
| HLI | rs4751178 |
| Exac | rs4751178 |
| Gnomad | rs4751178 |
| Varsome | rs4751178 |
| LitVar | rs4751178 |
| Map | rs4751178 |
| PheGenI | rs4751178 |
| Biobank | rs4751178 |
| 1000 genomes | rs4751178 |
| hgdp | rs4751178 |
| ensembl | rs4751178 |
| geneview | rs4751178 |
| scholar | rs4751178 |
| rs4751178 | |
| pharmgkb | rs4751178 |
| gwascentral | rs4751178 |
| openSNP | rs4751178 |
| 23andMe | rs4751178 |
| SNPshot | rs4751178 |
| SNPdbe | rs4751178 |
| MSV3d | rs4751178 |
| GWAS Ctlg | rs4751178 |
| GMAF | 0.2769 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19786962] |
| Trait | Speech perception in dyslexia |
| Title | First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children |
| Risk Allele | G |
| P-val | 0.000007 |
| Odds Ratio | NR NR |
