rs12022452
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12022452(A;A) |
| Make rs12022452(A;G) |
| Make rs12022452(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 40487628 |
| Gene | LOC105378672, ZFP69 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12022452 |
| dbSNP (classic) | rs12022452 |
| ClinGen | rs12022452 |
| ebi | rs12022452 |
| HLI | rs12022452 |
| Exac | rs12022452 |
| Gnomad | rs12022452 |
| Varsome | rs12022452 |
| LitVar | rs12022452 |
| Map | rs12022452 |
| PheGenI | rs12022452 |
| Biobank | rs12022452 |
| 1000 genomes | rs12022452 |
| hgdp | rs12022452 |
| ensembl | rs12022452 |
| geneview | rs12022452 |
| scholar | rs12022452 |
| rs12022452 | |
| pharmgkb | rs12022452 |
| gwascentral | rs12022452 |
| openSNP | rs12022452 |
| 23andMe | rs12022452 |
| SNPshot | rs12022452 |
| SNPdbe | rs12022452 |
| MSV3d | rs12022452 |
| GWAS Ctlg | rs12022452 |
| Max Magnitude | 0 |
| 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 | 1E-9 |
| Odds Ratio | NR NR |
