rs764256655
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs764256655(G;T) |
| Make rs764256655(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 197328935 |
| Gene | CRB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs764256655 |
| dbSNP (classic) | rs764256655 |
| ClinGen | rs764256655 |
| ebi | rs764256655 |
| HLI | rs764256655 |
| Exac | rs764256655 |
| Gnomad | rs764256655 |
| Varsome | rs764256655 |
| LitVar | rs764256655 |
| Map | rs764256655 |
| PheGenI | rs764256655 |
| Biobank | rs764256655 |
| 1000 genomes | rs764256655 |
| hgdp | rs764256655 |
| ensembl | rs764256655 |
| geneview | rs764256655 |
| scholar | rs764256655 |
| rs764256655 | |
| pharmgkb | rs764256655 |
| gwascentral | rs764256655 |
| openSNP | rs764256655 |
| 23andMe | rs764256655 |
| SNPshot | rs764256655 |
| SNPdbe | rs764256655 |
| MSV3d | rs764256655 |
| GWAS Ctlg | rs764256655 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs764256655(T;T) |
| Alt | rs764256655(T;T) |
| Reference | Rs764256655(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CRB1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.197298065G>T |
| CLNSRC | |
| CLNACC | RCV000255600.1, |
