rs771055145
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs771055145(A;G) |
| Make rs771055145(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 9 |
| Position | 12704577 |
| Gene | LURAP1L-AS1, TYRP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771055145 |
| dbSNP (classic) | rs771055145 |
| ClinGen | rs771055145 |
| ebi | rs771055145 |
| HLI | rs771055145 |
| Exac | rs771055145 |
| Gnomad | rs771055145 |
| Varsome | rs771055145 |
| LitVar | rs771055145 |
| Map | rs771055145 |
| PheGenI | rs771055145 |
| Biobank | rs771055145 |
| 1000 genomes | rs771055145 |
| hgdp | rs771055145 |
| ensembl | rs771055145 |
| geneview | rs771055145 |
| scholar | rs771055145 |
| rs771055145 | |
| pharmgkb | rs771055145 |
| gwascentral | rs771055145 |
| openSNP | rs771055145 |
| 23andMe | rs771055145 |
| SNPshot | rs771055145 |
| SNPdbe | rs771055145 |
| MSV3d | rs771055145 |
| GWAS Ctlg | rs771055145 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs771055145(G;G) |
| Alt | rs771055145(G;G) |
| Reference | Rs771055145(A;A) |
| Significance | Probable-Pathogenic |
| Disease | Ocular albinism |
| Variation | info |
| Gene | TYRP1 LURAP1L-AS1 |
| CLNDBN | Ocular albinism |
| Reversed | 0 |
| HGVS | NC_000009.11:g.12704577A>G |
| CLNSRC | |
| CLNACC | RCV000414933.1, |
