rs2038137
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2038137(A;A) |
| Make rs2038137(A;C) |
| Make rs2038137(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 24645715 |
| Gene | KIAA0319 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2038137 |
| dbSNP (classic) | rs2038137 |
| ClinGen | rs2038137 |
| ebi | rs2038137 |
| HLI | rs2038137 |
| Exac | rs2038137 |
| Gnomad | rs2038137 |
| Varsome | rs2038137 |
| LitVar | rs2038137 |
| Map | rs2038137 |
| PheGenI | rs2038137 |
| Biobank | rs2038137 |
| 1000 genomes | rs2038137 |
| hgdp | rs2038137 |
| ensembl | rs2038137 |
| geneview | rs2038137 |
| scholar | rs2038137 |
| rs2038137 | |
| pharmgkb | rs2038137 |
| gwascentral | rs2038137 |
| openSNP | rs2038137 |
| 23andMe | rs2038137 |
| SNPshot | rs2038137 |
| SNPdbe | rs2038137 |
| MSV3d | rs2038137 |
| GWAS Ctlg | rs2038137 |
| GMAF | 0.2484 |
| Max Magnitude | 0 |
[PMID 15514892
] A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
[PMID 15717286] Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
[PMID 16385449] Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
[PMID 19325871] A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
