rs62635654
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs62635654(C;T) |
| Make rs62635654(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 197427615 |
| Gene | CRB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62635654 |
| dbSNP (classic) | rs62635654 |
| ClinGen | rs62635654 |
| ebi | rs62635654 |
| HLI | rs62635654 |
| Exac | rs62635654 |
| Gnomad | rs62635654 |
| Varsome | rs62635654 |
| LitVar | rs62635654 |
| Map | rs62635654 |
| PheGenI | rs62635654 |
| Biobank | rs62635654 |
| 1000 genomes | rs62635654 |
| hgdp | rs62635654 |
| ensembl | rs62635654 |
| geneview | rs62635654 |
| scholar | rs62635654 |
| rs62635654 | |
| pharmgkb | rs62635654 |
| gwascentral | rs62635654 |
| openSNP | rs62635654 |
| 23andMe | rs62635654 |
| SNPshot | rs62635654 |
| SNPdbe | rs62635654 |
| MSV3d | rs62635654 |
| GWAS Ctlg | rs62635654 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs62635654(G;G) rs62635654(T;T) |
| Alt | rs62635654(G;G) rs62635654(T;T) |
| Reference | Rs62635654(C;C) |
| Significance | Pathogenic |
| Disease | Retinitis pigmentosa 12 not provided |
| Variation | info |
| Gene | CRB1 |
| CLNDBN | Retinitis pigmentosa 12 not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.197396745C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000006086.3, RCV000086317.1, |
