rs62236223
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs62236223(C;C) |
| Make rs62236223(C;T) |
| Make rs62236223(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 31467568 |
| Gene | EIF4ENIF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62236223 |
| dbSNP (classic) | rs62236223 |
| ClinGen | rs62236223 |
| ebi | rs62236223 |
| HLI | rs62236223 |
| Exac | rs62236223 |
| Gnomad | rs62236223 |
| Varsome | rs62236223 |
| LitVar | rs62236223 |
| Map | rs62236223 |
| PheGenI | rs62236223 |
| Biobank | rs62236223 |
| 1000 genomes | rs62236223 |
| hgdp | rs62236223 |
| ensembl | rs62236223 |
| geneview | rs62236223 |
| scholar | rs62236223 |
| rs62236223 | |
| pharmgkb | rs62236223 |
| gwascentral | rs62236223 |
| openSNP | rs62236223 |
| 23andMe | rs62236223 |
| SNPshot | rs62236223 |
| SNPdbe | rs62236223 |
| MSV3d | rs62236223 |
| GWAS Ctlg | rs62236223 |
| Max Magnitude | 0 |
| 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 | 7E-6 |
| Odds Ratio | .12 [NR] unit increase |
