rs749465098
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs749465098(C;T) |
| Make rs749465098(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 18142238 |
| Gene | MYO15A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs749465098 |
| dbSNP (classic) | rs749465098 |
| ClinGen | rs749465098 |
| ebi | rs749465098 |
| HLI | rs749465098 |
| Exac | rs749465098 |
| Gnomad | rs749465098 |
| Varsome | rs749465098 |
| LitVar | rs749465098 |
| Map | rs749465098 |
| PheGenI | rs749465098 |
| Biobank | rs749465098 |
| 1000 genomes | rs749465098 |
| hgdp | rs749465098 |
| ensembl | rs749465098 |
| geneview | rs749465098 |
| scholar | rs749465098 |
| rs749465098 | |
| pharmgkb | rs749465098 |
| gwascentral | rs749465098 |
| openSNP | rs749465098 |
| 23andMe | rs749465098 |
| SNPshot | rs749465098 |
| SNPdbe | rs749465098 |
| MSV3d | rs749465098 |
| GWAS Ctlg | rs749465098 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs749465098(T;T) |
| Alt | rs749465098(T;T) |
| Reference | Rs749465098(C;C) |
| Significance | Pathogenic |
| Disease | Deafness |
| Variation | info |
| Gene | MYO15A |
| CLNDBN | Deafness, autosomal recessive 3 |
| Reversed | 0 |
| HGVS | NC_000017.10:g.18045552C>T |
| CLNSRC | |
| CLNACC | RCV000230123.1, |
