rs4667193
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4667193(C;C) |
| Make rs4667193(C;T) |
| Make rs4667193(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 187761487 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4667193 |
| dbSNP (classic) | rs4667193 |
| ClinGen | rs4667193 |
| ebi | rs4667193 |
| HLI | rs4667193 |
| Exac | rs4667193 |
| Gnomad | rs4667193 |
| Varsome | rs4667193 |
| LitVar | rs4667193 |
| Map | rs4667193 |
| PheGenI | rs4667193 |
| Biobank | rs4667193 |
| 1000 genomes | rs4667193 |
| hgdp | rs4667193 |
| ensembl | rs4667193 |
| geneview | rs4667193 |
| scholar | rs4667193 |
| rs4667193 | |
| pharmgkb | rs4667193 |
| gwascentral | rs4667193 |
| openSNP | rs4667193 |
| 23andMe | rs4667193 |
| SNPshot | rs4667193 |
| SNPdbe | rs4667193 |
| MSV3d | rs4667193 |
| GWAS Ctlg | rs4667193 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24939585 ]
|
| Trait | Age-related hearing impairment (interaction) |
| Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
| Risk Allele | |
| P-val | 2E-9 |
| Odds Ratio | NR NR |
