rs9318086
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9318086(A;A) |
| Make rs9318086(A;G) |
| Make rs9318086(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 23858328 |
| Gene | MIPEP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9318086 |
| dbSNP (classic) | rs9318086 |
| ClinGen | rs9318086 |
| ebi | rs9318086 |
| HLI | rs9318086 |
| Exac | rs9318086 |
| Gnomad | rs9318086 |
| Varsome | rs9318086 |
| LitVar | rs9318086 |
| Map | rs9318086 |
| PheGenI | rs9318086 |
| Biobank | rs9318086 |
| 1000 genomes | rs9318086 |
| hgdp | rs9318086 |
| ensembl | rs9318086 |
| geneview | rs9318086 |
| scholar | rs9318086 |
| rs9318086 | |
| pharmgkb | rs9318086 |
| gwascentral | rs9318086 |
| openSNP | rs9318086 |
| 23andMe | rs9318086 |
| SNPshot | rs9318086 |
| SNPdbe | rs9318086 |
| MSV3d | rs9318086 |
| GWAS Ctlg | rs9318086 |
| GMAF | 0.4518 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21640322 ]
|
| Trait | |
| Title | Genetic variants at 13q12.12 are associated with high myopia in the han chinese population. |
| Risk Allele | A |
| P-val | 2E-16 |
| Odds Ratio | 1.3200 [1.19-1.46] |
[PMID 31300455] Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities.
