rs17822114
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs17822114(C;T) |
| Make rs17822114(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 60699699 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17822114 |
| dbSNP (classic) | rs17822114 |
| ClinGen | rs17822114 |
| ebi | rs17822114 |
| HLI | rs17822114 |
| Exac | rs17822114 |
| Gnomad | rs17822114 |
| Varsome | rs17822114 |
| LitVar | rs17822114 |
| Map | rs17822114 |
| PheGenI | rs17822114 |
| Biobank | rs17822114 |
| 1000 genomes | rs17822114 |
| hgdp | rs17822114 |
| ensembl | rs17822114 |
| geneview | rs17822114 |
| scholar | rs17822114 |
| rs17822114 | |
| pharmgkb | rs17822114 |
| gwascentral | rs17822114 |
| openSNP | rs17822114 |
| 23andMe | rs17822114 |
| SNPshot | rs17822114 |
| SNPdbe | rs17822114 |
| MSV3d | rs17822114 |
| GWAS Ctlg | rs17822114 |
| GMAF | 0.04454 |
| 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-18 |
| Odds Ratio | NR NR |
