rs11223996
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11223996(C;C) |
| Make rs11223996(C;T) |
| Make rs11223996(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 134756993 |
| Gene | HSFX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11223996 |
| dbSNP (classic) | rs11223996 |
| ClinGen | rs11223996 |
| ebi | rs11223996 |
| HLI | rs11223996 |
| Exac | rs11223996 |
| Gnomad | rs11223996 |
| Varsome | rs11223996 |
| LitVar | rs11223996 |
| Map | rs11223996 |
| PheGenI | rs11223996 |
| Biobank | rs11223996 |
| 1000 genomes | rs11223996 |
| hgdp | rs11223996 |
| ensembl | rs11223996 |
| geneview | rs11223996 |
| scholar | rs11223996 |
| rs11223996 | |
| pharmgkb | rs11223996 |
| gwascentral | rs11223996 |
| openSNP | rs11223996 |
| 23andMe | rs11223996 |
| SNPshot | rs11223996 |
| SNPdbe | rs11223996 |
| MSV3d | rs11223996 |
| GWAS Ctlg | rs11223996 |
| GMAF | 0.1056 |
| 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 | 7E-7 |
| Odds Ratio | NR NR |
