rs183589498
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs183589498(A;G) |
| Make rs183589498(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 63720822 |
| Gene | EYS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs183589498 |
| dbSNP (classic) | rs183589498 |
| ClinGen | rs183589498 |
| ebi | rs183589498 |
| HLI | rs183589498 |
| Exac | rs183589498 |
| Gnomad | rs183589498 |
| Varsome | rs183589498 |
| LitVar | rs183589498 |
| Map | rs183589498 |
| PheGenI | rs183589498 |
| Biobank | rs183589498 |
| 1000 genomes | rs183589498 |
| hgdp | rs183589498 |
| ensembl | rs183589498 |
| geneview | rs183589498 |
| scholar | rs183589498 |
| rs183589498 | |
| pharmgkb | rs183589498 |
| gwascentral | rs183589498 |
| openSNP | rs183589498 |
| 23andMe | rs183589498 |
| SNPshot | rs183589498 |
| SNPdbe | rs183589498 |
| MSV3d | rs183589498 |
| GWAS Ctlg | rs183589498 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs183589498(G;G) |
| Alt | rs183589498(G;G) |
| Reference | Rs183589498(A;A) |
| Significance | Pathogenic |
| Disease | Retinitis pigmentosa |
| Variation | info |
| Gene | EYS |
| CLNDBN | Retinitis pigmentosa |
| Reversed | 0 |
| HGVS | NC_000006.11:g.64430718A>G |
| CLNSRC | ClinVar |
| CLNACC | RCV000132637.1, |
