rs62636260
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs62636260(-;GT) |
| Make rs62636260(GT;GT) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 197328608 |
| Gene | CRB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62636260 |
| dbSNP (classic) | rs62636260 |
| ClinGen | rs62636260 |
| ebi | rs62636260 |
| HLI | rs62636260 |
| Exac | rs62636260 |
| Gnomad | rs62636260 |
| Varsome | rs62636260 |
| LitVar | rs62636260 |
| Map | rs62636260 |
| PheGenI | rs62636260 |
| Biobank | rs62636260 |
| 1000 genomes | rs62636260 |
| hgdp | rs62636260 |
| ensembl | rs62636260 |
| geneview | rs62636260 |
| scholar | rs62636260 |
| rs62636260 | |
| pharmgkb | rs62636260 |
| gwascentral | rs62636260 |
| openSNP | rs62636260 |
| 23andMe | rs62636260 |
| SNPshot | rs62636260 |
| SNPdbe | rs62636260 |
| MSV3d | rs62636260 |
| GWAS Ctlg | rs62636260 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs62636260(TG;TG) |
| Alt | rs62636260(TG;TG) |
| Reference | Rs62636260(-;-) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CRB1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.197297738_197297739dupTG |
| CLNSRC | |
| CLNACC | RCV000481076.2, |
