rs10758892
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10758892(A;A) |
Make rs10758892(A;G) |
Make rs10758892(G;G) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 9 |
Position | 7734250 |
is a | snp |
is | mentioned by |
dbSNP | rs10758892 |
dbSNP (classic) | rs10758892 |
ClinGen | rs10758892 |
ebi | rs10758892 |
HLI | rs10758892 |
Exac | rs10758892 |
Gnomad | rs10758892 |
Varsome | rs10758892 |
LitVar | rs10758892 |
Map | rs10758892 |
PheGenI | rs10758892 |
Biobank | rs10758892 |
1000 genomes | rs10758892 |
hgdp | rs10758892 |
ensembl | rs10758892 |
geneview | rs10758892 |
scholar | rs10758892 |
rs10758892 | |
pharmgkb | rs10758892 |
gwascentral | rs10758892 |
openSNP | rs10758892 |
23andMe | rs10758892 |
SNPshot | rs10758892 |
SNPdbe | rs10758892 |
MSV3d | rs10758892 |
GWAS Ctlg | rs10758892 |
GMAF | 0.1079 |
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 | 9E-6 |
Odds Ratio | NR NR |