rs2296781
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2296781(A;A) |
| Make rs2296781(A;G) |
| Make rs2296781(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 77429140 |
| Gene | GNA14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2296781 |
| dbSNP (classic) | rs2296781 |
| ClinGen | rs2296781 |
| ebi | rs2296781 |
| HLI | rs2296781 |
| Exac | rs2296781 |
| Gnomad | rs2296781 |
| Varsome | rs2296781 |
| LitVar | rs2296781 |
| Map | rs2296781 |
| PheGenI | rs2296781 |
| Biobank | rs2296781 |
| 1000 genomes | rs2296781 |
| hgdp | rs2296781 |
| ensembl | rs2296781 |
| geneview | rs2296781 |
| scholar | rs2296781 |
| rs2296781 | |
| pharmgkb | rs2296781 |
| gwascentral | rs2296781 |
| openSNP | rs2296781 |
| 23andMe | rs2296781 |
| SNPshot | rs2296781 |
| SNPdbe | rs2296781 |
| MSV3d | rs2296781 |
| GWAS Ctlg | rs2296781 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 5E-9 |
| Odds Ratio | NR NR |
