rs11145465
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11145465(A;A) |
Make rs11145465(A;C) |
Make rs11145465(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 69151677 |
Gene | TJP2 |
is a | snp |
is | mentioned by |
dbSNP | rs11145465 |
dbSNP (classic) | rs11145465 |
ClinGen | rs11145465 |
ebi | rs11145465 |
HLI | rs11145465 |
Exac | rs11145465 |
Gnomad | rs11145465 |
Varsome | rs11145465 |
LitVar | rs11145465 |
Map | rs11145465 |
PheGenI | rs11145465 |
Biobank | rs11145465 |
1000 genomes | rs11145465 |
hgdp | rs11145465 |
ensembl | rs11145465 |
geneview | rs11145465 |
scholar | rs11145465 |
rs11145465 | |
pharmgkb | rs11145465 |
gwascentral | rs11145465 |
openSNP | rs11145465 |
23andMe | rs11145465 |
SNPshot | rs11145465 |
SNPdbe | rs11145465 |
MSV3d | rs11145465 |
GWAS Ctlg | rs11145465 |
GMAF | 0.1322 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | A |
P-val | 7E-9 |
Odds Ratio | .12 [0.083-0.165] unit decrease |