rs10882165
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10882165(A;A) |
Make rs10882165(A;T) |
Make rs10882165(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 93164567 |
is a | snp |
is | mentioned by |
dbSNP | rs10882165 |
dbSNP (classic) | rs10882165 |
ClinGen | rs10882165 |
ebi | rs10882165 |
HLI | rs10882165 |
Exac | rs10882165 |
Gnomad | rs10882165 |
Varsome | rs10882165 |
LitVar | rs10882165 |
Map | rs10882165 |
PheGenI | rs10882165 |
Biobank | rs10882165 |
1000 genomes | rs10882165 |
hgdp | rs10882165 |
ensembl | rs10882165 |
geneview | rs10882165 |
scholar | rs10882165 |
rs10882165 | |
pharmgkb | rs10882165 |
gwascentral | rs10882165 |
openSNP | rs10882165 |
23andMe | rs10882165 |
SNPshot | rs10882165 |
SNPdbe | rs10882165 |
MSV3d | rs10882165 |
GWAS Ctlg | rs10882165 |
GMAF | 0.2888 |
Max Magnitude | 0 |
? | (A;A) (A;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-11 |
Odds Ratio | .11 [0.076-0.138] unit decrease |