rs1494630
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1494630(C;C) |
| Make rs1494630(C;T) |
| Make rs1494630(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 64098343 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1494630 |
| dbSNP (classic) | rs1494630 |
| ClinGen | rs1494630 |
| ebi | rs1494630 |
| HLI | rs1494630 |
| Exac | rs1494630 |
| Gnomad | rs1494630 |
| Varsome | rs1494630 |
| LitVar | rs1494630 |
| Map | rs1494630 |
| PheGenI | rs1494630 |
| Biobank | rs1494630 |
| 1000 genomes | rs1494630 |
| hgdp | rs1494630 |
| ensembl | rs1494630 |
| geneview | rs1494630 |
| scholar | rs1494630 |
| rs1494630 | |
| pharmgkb | rs1494630 |
| gwascentral | rs1494630 |
| openSNP | rs1494630 |
| 23andMe | rs1494630 |
| SNPshot | rs1494630 |
| SNPdbe | rs1494630 |
| MSV3d | rs1494630 |
| GWAS Ctlg | rs1494630 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24939585 ]
|
| Trait | Age-related hearing impairment |
| Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
| Risk Allele | |
| P-val | 1E-6 |
| Odds Ratio | .15 [NR] unit decrease |
