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.