rs133885
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 0 |
Make rs133885(A;A) |
Make rs133885(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 25763322 |
Gene | MYO18B |
is a | snp |
is | mentioned by |
dbSNP | rs133885 |
dbSNP (classic) | rs133885 |
ClinGen | rs133885 |
ebi | rs133885 |
HLI | rs133885 |
Exac | rs133885 |
Gnomad | rs133885 |
Varsome | rs133885 |
LitVar | rs133885 |
Map | rs133885 |
PheGenI | rs133885 |
Biobank | rs133885 |
1000 genomes | rs133885 |
hgdp | rs133885 |
ensembl | rs133885 |
geneview | rs133885 |
scholar | rs133885 |
rs133885 | |
pharmgkb | rs133885 |
gwascentral | rs133885 |
openSNP | rs133885 |
23andMe | rs133885 |
SNPshot | rs133885 |
SNPdbe | rs133885 |
MSV3d | rs133885 |
GWAS Ctlg | rs133885 |
GMAF | 0.3186 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23423138] |
Trait | Mathematical ability in children with dyslexia |
Title | A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. |
Risk Allele | |
P-val | 8E-10 |
Odds Ratio | 4.87 % increase |