rs12493123
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12493123(A;A) |
Make rs12493123(A;G) |
Make rs12493123(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 162351221 |
is a | snp |
is | mentioned by |
dbSNP | rs12493123 |
dbSNP (classic) | rs12493123 |
ClinGen | rs12493123 |
ebi | rs12493123 |
HLI | rs12493123 |
Exac | rs12493123 |
Gnomad | rs12493123 |
Varsome | rs12493123 |
LitVar | rs12493123 |
Map | rs12493123 |
PheGenI | rs12493123 |
Biobank | rs12493123 |
1000 genomes | rs12493123 |
hgdp | rs12493123 |
ensembl | rs12493123 |
geneview | rs12493123 |
scholar | rs12493123 |
rs12493123 | |
pharmgkb | rs12493123 |
gwascentral | rs12493123 |
openSNP | rs12493123 |
23andMe | rs12493123 |
SNPshot | rs12493123 |
SNPdbe | rs12493123 |
MSV3d | rs12493123 |
GWAS Ctlg | rs12493123 |
GMAF | 0.3453 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23738518] |
Trait | Reading and spelling |
Title | A genome-wide association study for reading and language abilities in two population cohorts. |
Risk Allele | |
P-val | 2E-6 |
Odds Ratio | NR NR |