rs611419
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs611419(A;A) |
| Make rs611419(A;T) |
| Make rs611419(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 8 |
| Position | 101491489 |
| Gene | GRHL2, LOC107986961, LOC107986962 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs611419 |
| dbSNP (classic) | rs611419 |
| ClinGen | rs611419 |
| ebi | rs611419 |
| HLI | rs611419 |
| Exac | rs611419 |
| Gnomad | rs611419 |
| Varsome | rs611419 |
| LitVar | rs611419 |
| Map | rs611419 |
| PheGenI | rs611419 |
| Biobank | rs611419 |
| 1000 genomes | rs611419 |
| hgdp | rs611419 |
| ensembl | rs611419 |
| geneview | rs611419 |
| scholar | rs611419 |
| rs611419 | |
| pharmgkb | rs611419 |
| gwascentral | rs611419 |
| openSNP | rs611419 |
| 23andMe | rs611419 |
| SNPshot | rs611419 |
| SNPdbe | rs611419 |
| MSV3d | rs611419 |
| GWAS Ctlg | rs611419 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 27318899] [Association between grainyhead-like 2 gene polymorphisms and noise-induced hearing loss].
