rs877098
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs877098(C;C) |
| Make rs877098(C;T) |
| Make rs877098(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 20224101 |
| Gene | GJB6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs877098 |
| dbSNP (classic) | rs877098 |
| ClinGen | rs877098 |
| ebi | rs877098 |
| HLI | rs877098 |
| Exac | rs877098 |
| Gnomad | rs877098 |
| Varsome | rs877098 |
| LitVar | rs877098 |
| Map | rs877098 |
| PheGenI | rs877098 |
| Biobank | rs877098 |
| 1000 genomes | rs877098 |
| hgdp | rs877098 |
| ensembl | rs877098 |
| geneview | rs877098 |
| scholar | rs877098 |
| rs877098 | |
| pharmgkb | rs877098 |
| gwascentral | rs877098 |
| openSNP | rs877098 |
| 23andMe | rs877098 |
| SNPshot | rs877098 |
| SNPdbe | rs877098 |
| MSV3d | rs877098 |
| GWAS Ctlg | rs877098 |
| GMAF | 0.4242 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20812880] The search of a genetic basis for noise-induced hearing loss (NIHL)
