rs12971120
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12971120(A;A) |
Make rs12971120(A;G) |
Make rs12971120(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 74506788 |
Gene | CNDP2 |
is a | snp |
is | mentioned by |
dbSNP | rs12971120 |
dbSNP (classic) | rs12971120 |
ClinGen | rs12971120 |
ebi | rs12971120 |
HLI | rs12971120 |
Exac | rs12971120 |
Gnomad | rs12971120 |
Varsome | rs12971120 |
LitVar | rs12971120 |
Map | rs12971120 |
PheGenI | rs12971120 |
Biobank | rs12971120 |
1000 genomes | rs12971120 |
hgdp | rs12971120 |
ensembl | rs12971120 |
geneview | rs12971120 |
scholar | rs12971120 |
rs12971120 | |
pharmgkb | rs12971120 |
gwascentral | rs12971120 |
openSNP | rs12971120 |
23andMe | rs12971120 |
SNPshot | rs12971120 |
SNPdbe | rs12971120 |
MSV3d | rs12971120 |
GWAS Ctlg | rs12971120 |
GMAF | 0.2043 |
Max Magnitude | 0 |
? | (A;A) (A;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 | G |
P-val | 2E-7 |
Odds Ratio | .10 [0.062-0.136] unit increase |