rs2521758
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2521758(G;G) |
| Make rs2521758(G;T) |
| Make rs2521758(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 7 |
| Position | 24722673 |
| Gene | DFNA5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2521758 |
| dbSNP (classic) | rs2521758 |
| ClinGen | rs2521758 |
| ebi | rs2521758 |
| HLI | rs2521758 |
| Exac | rs2521758 |
| Gnomad | rs2521758 |
| Varsome | rs2521758 |
| LitVar | rs2521758 |
| Map | rs2521758 |
| PheGenI | rs2521758 |
| Biobank | rs2521758 |
| 1000 genomes | rs2521758 |
| hgdp | rs2521758 |
| ensembl | rs2521758 |
| geneview | rs2521758 |
| scholar | rs2521758 |
| rs2521758 | |
| pharmgkb | rs2521758 |
| gwascentral | rs2521758 |
| openSNP | rs2521758 |
| 23andMe | rs2521758 |
| SNPshot | rs2521758 |
| SNPdbe | rs2521758 |
| MSV3d | rs2521758 |
| GWAS Ctlg | rs2521758 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26400775
] Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study
