rs4234898
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4234898(C;C) |
Make rs4234898(C;T) |
Make rs4234898(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 156077389 |
is a | snp |
is | mentioned by |
dbSNP | rs4234898 |
dbSNP (classic) | rs4234898 |
ClinGen | rs4234898 |
ebi | rs4234898 |
HLI | rs4234898 |
Exac | rs4234898 |
Gnomad | rs4234898 |
Varsome | rs4234898 |
LitVar | rs4234898 |
Map | rs4234898 |
PheGenI | rs4234898 |
Biobank | rs4234898 |
1000 genomes | rs4234898 |
hgdp | rs4234898 |
ensembl | rs4234898 |
geneview | rs4234898 |
scholar | rs4234898 |
rs4234898 | |
pharmgkb | rs4234898 |
gwascentral | rs4234898 |
openSNP | rs4234898 |
23andMe | rs4234898 |
SNPshot | rs4234898 |
SNPdbe | rs4234898 |
MSV3d | rs4234898 |
GWAS Ctlg | rs4234898 |
GMAF | 0.1331 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 5E-8 |
Odds Ratio | NR NR |