rs1656404
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1656404(C;C) |
Make rs1656404(C;T) |
Make rs1656404(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 232515231 |
is a | snp |
is | mentioned by |
dbSNP | rs1656404 |
dbSNP (classic) | rs1656404 |
ClinGen | rs1656404 |
ebi | rs1656404 |
HLI | rs1656404 |
Exac | rs1656404 |
Gnomad | rs1656404 |
Varsome | rs1656404 |
LitVar | rs1656404 |
Map | rs1656404 |
PheGenI | rs1656404 |
Biobank | rs1656404 |
1000 genomes | rs1656404 |
hgdp | rs1656404 |
ensembl | rs1656404 |
geneview | rs1656404 |
scholar | rs1656404 |
rs1656404 | |
pharmgkb | rs1656404 |
gwascentral | rs1656404 |
openSNP | rs1656404 |
23andMe | rs1656404 |
SNPshot | rs1656404 |
SNPdbe | rs1656404 |
MSV3d | rs1656404 |
GWAS Ctlg | rs1656404 |
GMAF | 0.1511 |
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 | A |
P-val | 8E-11 |
Odds Ratio | .15 [0.11-0.20] unit decrease |