rs11945798
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11945798(C;C) |
Make rs11945798(C;T) |
Make rs11945798(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 12767608 |
is a | snp |
is | mentioned by |
dbSNP | rs11945798 |
dbSNP (classic) | rs11945798 |
ClinGen | rs11945798 |
ebi | rs11945798 |
HLI | rs11945798 |
Exac | rs11945798 |
Gnomad | rs11945798 |
Varsome | rs11945798 |
LitVar | rs11945798 |
Map | rs11945798 |
PheGenI | rs11945798 |
Biobank | rs11945798 |
1000 genomes | rs11945798 |
hgdp | rs11945798 |
ensembl | rs11945798 |
geneview | rs11945798 |
scholar | rs11945798 |
rs11945798 | |
pharmgkb | rs11945798 |
gwascentral | rs11945798 |
openSNP | rs11945798 |
23andMe | rs11945798 |
SNPshot | rs11945798 |
SNPdbe | rs11945798 |
MSV3d | rs11945798 |
GWAS Ctlg | rs11945798 |
GMAF | 0.07484 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23738518] |
Trait | Word reading |
Title | A genome-wide association study for reading and language abilities in two population cohorts. |
Risk Allele | T |
P-val | 5E-6 |
Odds Ratio | .18 [0.1-0.25] unit decrease |