rs4792192
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4792192(C;C) |
| Make rs4792192(C;T) |
| Make rs4792192(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 11900144 |
| Gene | DNAH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4792192 |
| dbSNP (classic) | rs4792192 |
| ClinGen | rs4792192 |
| ebi | rs4792192 |
| HLI | rs4792192 |
| Exac | rs4792192 |
| Gnomad | rs4792192 |
| Varsome | rs4792192 |
| LitVar | rs4792192 |
| Map | rs4792192 |
| PheGenI | rs4792192 |
| Biobank | rs4792192 |
| 1000 genomes | rs4792192 |
| hgdp | rs4792192 |
| ensembl | rs4792192 |
| geneview | rs4792192 |
| scholar | rs4792192 |
| rs4792192 | |
| pharmgkb | rs4792192 |
| gwascentral | rs4792192 |
| openSNP | rs4792192 |
| 23andMe | rs4792192 |
| SNPshot | rs4792192 |
| SNPdbe | rs4792192 |
| MSV3d | rs4792192 |
| GWAS Ctlg | rs4792192 |
| GMAF | 0.3035 |
| 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 | 3E-6 |
| Odds Ratio | NR NR |
