rs3777781
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3777781(A;A) |
| Make rs3777781(A;T) |
| Make rs3777781(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 133247575 |
| Gene | EYA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3777781 |
| dbSNP (classic) | rs3777781 |
| ClinGen | rs3777781 |
| ebi | rs3777781 |
| HLI | rs3777781 |
| Exac | rs3777781 |
| Gnomad | rs3777781 |
| Varsome | rs3777781 |
| LitVar | rs3777781 |
| Map | rs3777781 |
| PheGenI | rs3777781 |
| Biobank | rs3777781 |
| 1000 genomes | rs3777781 |
| hgdp | rs3777781 |
| ensembl | rs3777781 |
| geneview | rs3777781 |
| scholar | rs3777781 |
| rs3777781 | |
| pharmgkb | rs3777781 |
| gwascentral | rs3777781 |
| openSNP | rs3777781 |
| 23andMe | rs3777781 |
| SNPshot | rs3777781 |
| SNPdbe | rs3777781 |
| MSV3d | rs3777781 |
| GWAS Ctlg | rs3777781 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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
