rs212769
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs212769(A;A) |
| Make rs212769(A;G) |
| Make rs212769(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 133452410 |
| Gene | EYA4, LOC107984121 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs212769 |
| dbSNP (classic) | rs212769 |
| ClinGen | rs212769 |
| ebi | rs212769 |
| HLI | rs212769 |
| Exac | rs212769 |
| Gnomad | rs212769 |
| Varsome | rs212769 |
| LitVar | rs212769 |
| Map | rs212769 |
| PheGenI | rs212769 |
| Biobank | rs212769 |
| 1000 genomes | rs212769 |
| hgdp | rs212769 |
| ensembl | rs212769 |
| geneview | rs212769 |
| scholar | rs212769 |
| rs212769 | |
| pharmgkb | rs212769 |
| gwascentral | rs212769 |
| openSNP | rs212769 |
| 23andMe | rs212769 |
| SNPshot | rs212769 |
| SNPdbe | rs212769 |
| MSV3d | rs212769 |
| GWAS Ctlg | rs212769 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26400775
] Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study
