rs12216812
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12216812(A;A) |
Make rs12216812(A;G) |
Make rs12216812(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 81239512 |
is a | snp |
is | mentioned by |
dbSNP | rs12216812 |
dbSNP (classic) | rs12216812 |
ClinGen | rs12216812 |
ebi | rs12216812 |
HLI | rs12216812 |
Exac | rs12216812 |
Gnomad | rs12216812 |
Varsome | rs12216812 |
LitVar | rs12216812 |
Map | rs12216812 |
PheGenI | rs12216812 |
Biobank | rs12216812 |
1000 genomes | rs12216812 |
hgdp | rs12216812 |
ensembl | rs12216812 |
geneview | rs12216812 |
scholar | rs12216812 |
rs12216812 | |
pharmgkb | rs12216812 |
gwascentral | rs12216812 |
openSNP | rs12216812 |
23andMe | rs12216812 |
SNPshot | rs12216812 |
SNPdbe | rs12216812 |
MSV3d | rs12216812 |
GWAS Ctlg | rs12216812 |
GMAF | 0.05005 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23049088] |
Trait | Myopia (pathological) |
Title | A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population. |
Risk Allele | |
P-val | 3E-9 |
Odds Ratio | NR NR |