rs121918561
From SNPedia
| Merged into | rs61755777 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (GCT;GCT) | 0 | common in clinvar |
| (TGC;TGC) | 0 | common/normal |
| Make rs121918561(-;-) |
| Make rs121918561(-;TGC) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 42721981 |
| Gene | PRPH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121918561 |
| dbSNP (classic) | rs121918561 |
| ClinGen | rs121918561 |
| ebi | rs121918561 |
| HLI | rs121918561 |
| Exac | rs121918561 |
| Gnomad | rs121918561 |
| Varsome | rs121918561 |
| LitVar | rs121918561 |
| Map | rs121918561 |
| PheGenI | rs121918561 |
| Biobank | rs121918561 |
| 1000 genomes | rs121918561 |
| hgdp | rs121918561 |
| ensembl | rs121918561 |
| geneview | rs121918561 |
| scholar | rs121918561 |
| rs121918561 | |
| pharmgkb | rs121918561 |
| gwascentral | rs121918561 |
| openSNP | rs121918561 |
| 23andMe | rs121918561 |
| SNPshot | rs121918561 |
| SNPdbe | rs121918561 |
| MSV3d | rs121918561 |
| GWAS Ctlg | rs121918561 |
| Status | Merged into rs61755777 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs121918561(GCT;GCT) |
| Significance | Pathogenic |
| Disease | Retinitis pigmentosa 7 not provided |
| Variation | info |
| Gene | PRPH2 |
| CLNDBN | Retinitis pigmentosa 7 not provided |
| Reversed | 1 |
| HGVS | NC_000006.11:g.42689715_42689717delAGC |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000014048.24, RCV000084963.1, |
