rs4462272
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4462272(C;C) |
| Make rs4462272(C;T) |
| Make rs4462272(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 100063786 |
| Gene | CPN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4462272 |
| dbSNP (classic) | rs4462272 |
| ClinGen | rs4462272 |
| ebi | rs4462272 |
| HLI | rs4462272 |
| Exac | rs4462272 |
| Gnomad | rs4462272 |
| Varsome | rs4462272 |
| LitVar | rs4462272 |
| Map | rs4462272 |
| PheGenI | rs4462272 |
| Biobank | rs4462272 |
| 1000 genomes | rs4462272 |
| hgdp | rs4462272 |
| ensembl | rs4462272 |
| geneview | rs4462272 |
| scholar | rs4462272 |
| rs4462272 | |
| pharmgkb | rs4462272 |
| gwascentral | rs4462272 |
| openSNP | rs4462272 |
| 23andMe | rs4462272 |
| SNPshot | rs4462272 |
| SNPdbe | rs4462272 |
| MSV3d | rs4462272 |
| GWAS Ctlg | rs4462272 |
| 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 | 8E-9 |
| Odds Ratio | NR NR |
