rs6111803
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs6111803(G;T) |
| Make rs6111803(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 18041718 |
| Gene | OVOL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6111803 |
| dbSNP (classic) | rs6111803 |
| ClinGen | rs6111803 |
| ebi | rs6111803 |
| HLI | rs6111803 |
| Exac | rs6111803 |
| Gnomad | rs6111803 |
| Varsome | rs6111803 |
| LitVar | rs6111803 |
| Map | rs6111803 |
| PheGenI | rs6111803 |
| Biobank | rs6111803 |
| 1000 genomes | rs6111803 |
| hgdp | rs6111803 |
| ensembl | rs6111803 |
| geneview | rs6111803 |
| scholar | rs6111803 |
| rs6111803 | |
| pharmgkb | rs6111803 |
| gwascentral | rs6111803 |
| openSNP | rs6111803 |
| 23andMe | rs6111803 |
| SNPshot | rs6111803 |
| SNPdbe | rs6111803 |
| MSV3d | rs6111803 |
| GWAS Ctlg | rs6111803 |
| GMAF | 0.03444 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19574904
] Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval
