rs61754382
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of a tyrosinase-negative oculocutaneous albinism mutation |
| (G;G) | 0 | common/normal |
| Make rs61754382(A;A) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 89227822 |
| Gene | LOC107984363, TYR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61754382 |
| dbSNP (classic) | rs61754382 |
| ClinGen | rs61754382 |
| ebi | rs61754382 |
| HLI | rs61754382 |
| Exac | rs61754382 |
| Gnomad | rs61754382 |
| Varsome | rs61754382 |
| LitVar | rs61754382 |
| Map | rs61754382 |
| PheGenI | rs61754382 |
| Biobank | rs61754382 |
| 1000 genomes | rs61754382 |
| hgdp | rs61754382 |
| ensembl | rs61754382 |
| geneview | rs61754382 |
| scholar | rs61754382 |
| rs61754382 | |
| pharmgkb | rs61754382 |
| gwascentral | rs61754382 |
| openSNP | rs61754382 |
| 23andMe | rs61754382 |
| SNPshot | rs61754382 |
| SNPdbe | rs61754382 |
| MSV3d | rs61754382 |
| GWAS Ctlg | rs61754382 |
| Max Magnitude | 3 |
aka c.1037-1G>A
