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 |
