rs761100
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 1 | higher risk for dyslexia |
| (G;T) | 0 | normal risk |
| (T;T) | 0 | normal risk |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 24632414 |
| Gene | KIAA0319 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761100 |
| dbSNP (classic) | rs761100 |
| ClinGen | rs761100 |
| ebi | rs761100 |
| HLI | rs761100 |
| Exac | rs761100 |
| Gnomad | rs761100 |
| Varsome | rs761100 |
| LitVar | rs761100 |
| Map | rs761100 |
| PheGenI | rs761100 |
| Biobank | rs761100 |
| 1000 genomes | rs761100 |
| hgdp | rs761100 |
| ensembl | rs761100 |
| geneview | rs761100 |
| scholar | rs761100 |
| rs761100 | |
| pharmgkb | rs761100 |
| gwascentral | rs761100 |
| openSNP | rs761100 |
| 23andMe | rs761100 |
| SNPshot | rs761100 |
| SNPdbe | rs761100 |
| MSV3d | rs761100 |
| GWAS Ctlg | rs761100 |
| GMAF | 0.3173 |
| Max Magnitude | 1 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
The more common allele of rs761100 has been linked to increased risk for developmental dyslexia in a study of ~300 British families. While odds ratios were not reported, the significance was reported as p=0.02.[PMID 17033633]
[PMID 19997522
] Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.
