rs577948
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs577948(A;A) |
| Make rs577948(A;G) |
| Make rs577948(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 122159482 |
| Gene | MIR100HG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs577948 |
| dbSNP (classic) | rs577948 |
| ClinGen | rs577948 |
| ebi | rs577948 |
| HLI | rs577948 |
| Exac | rs577948 |
| Gnomad | rs577948 |
| Varsome | rs577948 |
| LitVar | rs577948 |
| Map | rs577948 |
| PheGenI | rs577948 |
| Biobank | rs577948 |
| 1000 genomes | rs577948 |
| hgdp | rs577948 |
| ensembl | rs577948 |
| geneview | rs577948 |
| scholar | rs577948 |
| rs577948 | |
| pharmgkb | rs577948 |
| gwascentral | rs577948 |
| openSNP | rs577948 |
| 23andMe | rs577948 |
| SNPshot | rs577948 |
| SNPdbe | rs577948 |
| MSV3d | rs577948 |
| GWAS Ctlg | rs577948 |
| GMAF | 0.3632 |
| Max Magnitude | 0 |
Despite two previous GWAS studies associating this SNP with high myopia in Japanese populations, no association was seen in a Chinese population studied.[PMID 22194655
]
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19779542]
|
| Trait | Myopia (pathological) |
| Title | A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1 |
| Risk Allele | G |
| P-val | 2E-7 |
| Odds Ratio | 1.37 [1.21-1.54] |
