rs17648524
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17648524(C;C) |
Make rs17648524(C;G) |
Make rs17648524(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 7409682 |
Gene | RBFOX1 |
is a | snp |
is | mentioned by |
dbSNP | rs17648524 |
dbSNP (classic) | rs17648524 |
ClinGen | rs17648524 |
ebi | rs17648524 |
HLI | rs17648524 |
Exac | rs17648524 |
Gnomad | rs17648524 |
Varsome | rs17648524 |
LitVar | rs17648524 |
Map | rs17648524 |
PheGenI | rs17648524 |
Biobank | rs17648524 |
1000 genomes | rs17648524 |
hgdp | rs17648524 |
ensembl | rs17648524 |
geneview | rs17648524 |
scholar | rs17648524 |
rs17648524 | |
pharmgkb | rs17648524 |
gwascentral | rs17648524 |
openSNP | rs17648524 |
23andMe | rs17648524 |
SNPshot | rs17648524 |
SNPdbe | rs17648524 |
MSV3d | rs17648524 |
GWAS Ctlg | rs17648524 |
GMAF | 0.2268 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23396134] |
Trait | Refractive error |
Title | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. |
Risk Allele | C |
P-val | 6E-10 |
Odds Ratio | .12 [0.081-0.155] unit decrease |