rs854777
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs854777(A;G) |
| Make rs854777(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 18143584 |
| Gene | MYO15A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs854777 |
| dbSNP (classic) | rs854777 |
| ClinGen | rs854777 |
| ebi | rs854777 |
| HLI | rs854777 |
| Exac | rs854777 |
| Gnomad | rs854777 |
| Varsome | rs854777 |
| LitVar | rs854777 |
| Map | rs854777 |
| PheGenI | rs854777 |
| Biobank | rs854777 |
| 1000 genomes | rs854777 |
| hgdp | rs854777 |
| ensembl | rs854777 |
| geneview | rs854777 |
| scholar | rs854777 |
| rs854777 | |
| pharmgkb | rs854777 |
| gwascentral | rs854777 |
| openSNP | rs854777 |
| 23andMe | rs854777 |
| SNPshot | rs854777 |
| SNPdbe | rs854777 |
| MSV3d | rs854777 |
| GWAS Ctlg | rs854777 |
| GMAF | 0.2466 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18776599
] Susceptibility genes for gentamicin-induced vestibular dysfunction.
| ClinVar | |
|---|---|
| Risk | rs854777(G;G) |
| Alt | rs854777(G;G) |
| Reference | Rs854777(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Nonsyndromic Hearing Loss |
| Variation | info |
| Gene | MYO15A |
| CLNDBN | not specified Nonsyndromic Hearing Loss, Recessive |
| Reversed | 1 |
| HGVS | NC_000017.10:g.18046898T>C |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000038976.4, RCV000311460.1, |
