rs1559777
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1559777(C;C) |
| Make rs1559777(C;T) |
| Make rs1559777(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 57788419 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1559777 |
| dbSNP (classic) | rs1559777 |
| ClinGen | rs1559777 |
| ebi | rs1559777 |
| HLI | rs1559777 |
| Exac | rs1559777 |
| Gnomad | rs1559777 |
| Varsome | rs1559777 |
| LitVar | rs1559777 |
| Map | rs1559777 |
| PheGenI | rs1559777 |
| Biobank | rs1559777 |
| 1000 genomes | rs1559777 |
| hgdp | rs1559777 |
| ensembl | rs1559777 |
| geneview | rs1559777 |
| scholar | rs1559777 |
| rs1559777 | |
| pharmgkb | rs1559777 |
| gwascentral | rs1559777 |
| openSNP | rs1559777 |
| 23andMe | rs1559777 |
| SNPshot | rs1559777 |
| SNPdbe | rs1559777 |
| MSV3d | rs1559777 |
| GWAS Ctlg | rs1559777 |
| GMAF | 0.2769 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 1E-6 |
| Odds Ratio | NR NR |
