rs17183295
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17183295(C;C) |
Make rs17183295(C;T) |
Make rs17183295(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 32751254 |
Gene | MYO1D |
is a | snp |
is | mentioned by |
dbSNP | rs17183295 |
dbSNP (classic) | rs17183295 |
ClinGen | rs17183295 |
ebi | rs17183295 |
HLI | rs17183295 |
Exac | rs17183295 |
Gnomad | rs17183295 |
Varsome | rs17183295 |
LitVar | rs17183295 |
Map | rs17183295 |
PheGenI | rs17183295 |
Biobank | rs17183295 |
1000 genomes | rs17183295 |
hgdp | rs17183295 |
ensembl | rs17183295 |
geneview | rs17183295 |
scholar | rs17183295 |
rs17183295 | |
pharmgkb | rs17183295 |
gwascentral | rs17183295 |
openSNP | rs17183295 |
23andMe | rs17183295 |
SNPshot | rs17183295 |
SNPdbe | rs17183295 |
MSV3d | rs17183295 |
GWAS Ctlg | rs17183295 |
GMAF | 0.0955 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 1E-10 |
Odds Ratio | .13 [0.092-0.17] unit decrease |