rs281865525
From SNPedia
| Merged into | rs61754361 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs281865525(-;-) |
| Make rs281865525(-;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 89178525 |
| Gene | TYR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs281865525 |
| dbSNP (classic) | rs281865525 |
| ClinGen | rs281865525 |
| ebi | rs281865525 |
| HLI | rs281865525 |
| Exac | rs281865525 |
| Gnomad | rs281865525 |
| Varsome | rs281865525 |
| LitVar | rs281865525 |
| Map | rs281865525 |
| PheGenI | rs281865525 |
| Biobank | rs281865525 |
| 1000 genomes | rs281865525 |
| hgdp | rs281865525 |
| ensembl | rs281865525 |
| geneview | rs281865525 |
| scholar | rs281865525 |
| rs281865525 | |
| pharmgkb | rs281865525 |
| gwascentral | rs281865525 |
| openSNP | rs281865525 |
| 23andMe | rs281865525 |
| SNPshot | rs281865525 |
| SNPdbe | rs281865525 |
| MSV3d | rs281865525 |
| GWAS Ctlg | rs281865525 |
| Status | Merged into rs61754361 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs281865525(G;G) |
| Significance | Pathogenic |
| Disease | Tyrosinase-negative oculocutaneous albinism not provided |
| Variation | info |
| Gene | TYR |
| CLNDBN | Tyrosinase-negative oculocutaneous albinism not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.88911693delG |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000003988.2, RCV000085954.1, |
